17-16343428-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343428
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343427
    reference: chr 17
allele count: 4
allele frequency: 3.296522169111587e-5
allele num: 121340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.165-70delG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.207-70delG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.89-70delG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.265-70delG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.97delG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.271-70delG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.415-70delG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.89-70delG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.113-70delG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.251delG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.96-70delG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.839delG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.113-70delG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.212-70delG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.164-70delG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.378-70delG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.112-70delG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.379-70delG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.267-70delG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.109-70delG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.161delG
  variant of: http://identifiers.org/hgnc/28619
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: AG
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

17-16343428-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343428
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343428
    reference: chr 17
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.529-71A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.297-71A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.379-71A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.378-71A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.113-71A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.379-71A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.96-71A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.207-71A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.212-71A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.250A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.838A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.645A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.109-71A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.68-71A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.271-71A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.89-71A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.160A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.267-71A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.212-71A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.265-71A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.89-71A>T
  variant of: http://identifiers.org/hgnc/28619
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

17-16343433-TCAC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343433
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343430
    reference: chr 17
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.297-62_297-60delCAC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.109-62_109-60delCAC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.169_171delCAC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.165-62_165-60delCAC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.105_107delCAC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.529-62_529-60delCAC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.379-62_379-60delCAC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.654_656delCAC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.847_849delCAC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.113-62_113-60delCAC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.265-62_265-60delCAC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.68-62_68-60delCAC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.259_261delCAC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.207-62_207-60delCAC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.378-62_378-60delCAC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.212-62_212-60delCAC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.96-62_96-60delCAC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.357-62_357-60delCAC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.89-62_89-60delCAC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.265-62_265-60delCAC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.112-62_112-60delCAC
  variant of: http://identifiers.org/hgnc/28619
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: TCAC
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

17-16343434-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343434
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343434
    reference: chr 17
allele count: 4
allele frequency: 3.296033224014898e-5
allele num: 121358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.651C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.529-65C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.96-65C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.265-65C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.379-65C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.165-65C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.844C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.102C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.379-65C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.89-65C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.212-65C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.256C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.357-65C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.112-65C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.113-65C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.271-65C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.297-65C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.68-65C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.265-65C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.378-65C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.89-65C>T
  variant of: http://identifiers.org/hgnc/28619
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

17-16343442-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343442
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343442
    reference: chr 17
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.212-57G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.113-57G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.110G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.271-57G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.529-57G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.265-57G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.96-57G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.659G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.89-57G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.379-57G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.264G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.265-57G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.207-57G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.165-57G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.852G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.379-57G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.212-57G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.415-57G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.267-57G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.109-57G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.112-57G>C
  variant of: http://identifiers.org/hgnc/28619
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

17-16343451-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343451
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343451
    reference: chr 17
allele count: 13
allele frequency: 1.070981348447901e-4
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.273C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.861C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.89-48C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.165-48C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.265-48C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.89-48C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.415-48C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.212-48C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.668C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.379-48C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.183C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.207-48C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.164-48C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.109-48C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.68-48C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.119C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.297-48C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.265-48C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.212-48C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.113-48C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.271-48C>T
  variant of: http://identifiers.org/hgnc/28619
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

17-16343452-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343452
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343452
    reference: chr 17
allele count: 2
allele frequency: 1.647609318878308e-5
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.112-47A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.378-47A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.415-47A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.265-47A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.164-47A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.669A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.113-47A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.265-47A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.165-47A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.379-47A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.89-47A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.120A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.113-47A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.274A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.184A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.212-47A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.68-47A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.862A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.271-47A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.109-47A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.212-47A>G
  variant of: http://identifiers.org/hgnc/28619
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

17-16343455-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343455
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343455
    reference: chr 17
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.212-44A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.271-44A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.672A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.212-44A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.109-44A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.89-44A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.379-44A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.865A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.113-44A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.123A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.267-44A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.112-44A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.265-44A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.187A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.265-44A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.277A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.165-44A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.415-44A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.357-44A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.89-44A>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.113-44A>T
  variant of: http://identifiers.org/hgnc/28619
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

17-16343463-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343463
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343463
    reference: chr 17
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.68-36T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.113-36T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.415-36T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.873T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.265-36T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.96-36T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.379-36T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.357-36T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.285T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.379-36T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.112-36T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.680T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.131T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.212-36T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.297-36T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.207-36T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.529-36T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.113-36T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.89-36T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.265-36T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.378-36T>G
  variant of: http://identifiers.org/hgnc/28619
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/17-16343469-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343469
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343469
    reference: chr 17
allele count: 100
allele frequency: 8.237910865804432e-4
allele num: 121390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.267-30A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.165-30A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.137A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.113-30A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.68-30A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.378-30A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.89-30A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.379-30A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.212-30A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.357-30A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.686A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.879A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.212-30A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.271-30A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.201A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.207-30A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.112-30A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.113-30A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.529-30A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.297-30A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.164-30A>C
  variant of: http://identifiers.org/hgnc/28619
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/17-16343477-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343477
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343477
    reference: chr 17
allele count: 3
allele frequency: 2.47137325974133e-5
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.89-22C>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.68-22C>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.212-22C>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.265-22C>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.212-22C>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.207-22C>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.887C>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.113-22C>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.145C>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.113-22C>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.96-22C>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.109-22C>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.209C>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.164-22C>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.379-22C>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.378-22C>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.694C>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.415-22C>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.297-22C>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.112-22C>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.357-22C>A
  variant of: http://identifiers.org/hgnc/28619
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

17-16343483-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343483
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343483
    reference: chr 17
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.113-16T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.215T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.265-16T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.379-16T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.893T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.700T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.164-16T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.271-16T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.267-16T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.109-16T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.207-16T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.378-16T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.297-16T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.89-16T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.212-16T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.357-16T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.379-16T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.113-16T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.151T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.165-16T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.265-16T>A
  variant of: http://identifiers.org/hgnc/28619
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

17-16343487-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343487
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343487
    reference: chr 17
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.529-12A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.89-12A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.113-12A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.207-12A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.96-12A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.219A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.415-12A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.165-12A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.267-12A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.297-12A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.155A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.113-12A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.378-12A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.897A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.379-12A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.89-12A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.309A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.212-12A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.704A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.112-12A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.265-12A>G
  variant of: http://identifiers.org/hgnc/28619
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff

17-16343489-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343489
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343489
    reference: chr 17
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.112-10A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.378-10A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.89-10A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.221A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.357-10A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.379-10A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.706A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.212-10A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.529-10A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.109-10A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.207-10A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.415-10A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.899A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.157A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.164-10A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.68-10A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.113-10A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.165-10A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.271-10A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.267-10A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.311A>G
  variant of: http://identifiers.org/hgnc/28619
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP

17-16343489-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343489
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343488
    reference: chr 17
allele count: 4
allele frequency: 3.295164346321773e-5
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.96-8delT
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.159delT
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.708delT
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.113-8delT
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.901delT
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.223delT
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.265-8delT
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.378-8delT
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.379-8delT
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.109-8delT
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.313delT
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.357-8delT
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.271-8delT
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.415-8delT
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.164-8delT
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.267-8delT
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.165-8delT
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.529-8delT
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.113-8delT
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.89-8delT
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.297-8delT
  variant of: http://identifiers.org/hgnc/28619
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: AT
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

17-16343500-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343500
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343500
    reference: chr 17
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.69T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.213T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.416T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.379T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.166T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.232T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.110T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.165T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.530T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.114T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.266T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.358T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.272T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.114T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.910T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.97T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.380T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.90T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.213T>A
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: n.208T>A
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD

17-16343500-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343500
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343500
    reference: chr 17
allele count: 2
allele frequency: 1.647500741375333e-5
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.266T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.380T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.166T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.213T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.90T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.266T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.358T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.717T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.97T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.298T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.530T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.114T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.213T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.113T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.380T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.69T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.272T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.168T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.322T>C
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: n.208T>C
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

17-16343502-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343502
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343502
    reference: chr 17
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.112G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.381G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.99G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.270G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.274G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.71G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.912G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.170G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.324G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.382G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.382G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.115G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.167G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.418G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.168G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.215G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.215G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.210G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.116G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.92G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.116G>A
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

17-16343513-AAGAATC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343513
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343507
    reference: chr 17
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.130_135delAATCAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.396_401delAATCAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.184_189delAATCAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.432_437delAATCAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.229_234delAATCAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.85_90delAATCAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.314_319delAATCAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.130_135delAATCAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.396_401delAATCAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.733_738delAATCAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.126_131delAATCAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.106_111delAATCAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.248_253delAATCAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.129_134delAATCAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.395_400delAATCAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.181_186delAATCAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.182_187delAATCAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.113_118delAATCAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.288_293delAATCAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.374_379delAATCAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.284_289delAATCAG
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: AAGAATC
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

17-16343520-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343520
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343520
    reference: chr 17
allele count: 3
allele frequency: 2.47137325974133e-5
allele num: 121390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.130A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.188A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.233A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.134A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.436A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.400A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.286A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.186A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.550A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.252A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.737A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.318A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.185A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.117A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.133A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.292A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.89A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.228A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.930A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.134A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.110A>G
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

17-16343527-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343527
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343527
    reference: chr 17
allele count: 6
allele frequency: 4.94266508501384e-5
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.117T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.259T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.407T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.443T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.293T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.299T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.295T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.385T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.937T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.137T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.406T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.195T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.193T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.117T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.325T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.140T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.124T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.349T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.557T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.240T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.141T>A
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

17-16343529-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343529
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343529
    reference: chr 17
allele count: 13
allele frequency: 1.070928412554576e-4
allele num: 121390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.409T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.242T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.746T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.409T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.119T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.387T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.445T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.142T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.195T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.301T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.939T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.297T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.143T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.98T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.351T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.261T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.126T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.408T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.143T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.194T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.197T>C
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

17-16343530-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343530
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343530
    reference: chr 17
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.328T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.196T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.140T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.198T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.243T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.298T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.144T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.410T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.446T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.195T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.747T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.410T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.302T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.262T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.143T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.127T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.352T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.120T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.940T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.296T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.120T>C
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP

17-16343543-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343543
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343543
    reference: chr 17
allele count: 2
allele frequency: 1.647717910693689e-5
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.275A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.315A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.256A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.341A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.422A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.209A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.153A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.140A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.953A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.157A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.112A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.251A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.459A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.311A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.423A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.365A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.423A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.156A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.256A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.760A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.208A>G
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum

17-16343545-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343545
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343545
    reference: chr 17
allele count: 2
allele frequency: 1.64774506088418e-5
allele num: 121378
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.135T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.155T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.258T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.253T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.311T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.258T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.277T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.425T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.142T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.159T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.210T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.211T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.313T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.403T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.159T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.424T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.425T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.317T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.955T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.213T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.114T>C
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

17-16343546-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343546
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343546
    reference: chr 17
allele count: 3
allele frequency: 2.471780505891077e-5
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.956G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.425G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.312G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.462G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.404G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.159G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.115G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.426G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.160G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.136G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.212G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.143G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.318G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.160G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.259G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.314G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.312G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.278G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.211G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.763G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.214G>A
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

17-16343547-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343547
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343547
    reference: chr 17
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.116G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.160G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.315G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.577G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.255G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.137G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.212G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.161G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.463G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.426G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.427G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.957G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.319G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.144G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.157G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.215G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.405G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.260G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.369G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.427G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.161G>A
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

17-16343556-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343556
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343556
    reference: chr 17
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.169G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.153G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.435G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.170G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.773G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.269G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.288G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.436G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.966G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.324G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.221G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.166G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.224G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.125G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.436G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.322G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.328G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.222G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.378G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.322G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.354G>A
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD

17-16343563-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343563
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343563
    reference: chr 17
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.231A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.593A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.443A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.176A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.479A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.229A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.271A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.132A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.335A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.177A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.385A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.160A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.153A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.177A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.331A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.153A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.276A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.228A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.173A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.295A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.361A>G
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS

17-16343564-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343564
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343564
    reference: chr 17
allele count: 2
allele frequency: 1.648179585647652e-5
allele num: 121346
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.154T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.332T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.330T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.272T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.781T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.232T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.229T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.177T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.480T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.178T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.277T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.336T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.386T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.161T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.133T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.296T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.230T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.174T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.422T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.330T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.444T>C
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD

17-16343567-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343567
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343567
    reference: chr 17
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.280G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.177G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.597G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.389G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.275G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.157G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.164G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.181G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.446G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.233G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.181G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.235G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.977G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.483G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.299G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.339G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.784G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.180G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.335G>A
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: n.275G>A
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD

17-16343570-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343570
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343570
    reference: chr 17
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.446+3A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.232+3A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.333+3A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.447+3A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.447+3A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.389+3A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.235+3A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.181+3A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.335+3A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.299+3A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.177+3A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.180+3A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.164+3A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.784+3A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.233+3A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.365+3A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.339+3A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.157+3A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.483+3A>G
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: n.275+3A>G
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/17-16343571-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343571
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343571
    reference: chr 17
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.232+4A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.483+4A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.280+4A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.365+4A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.339+4A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.447+4A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.235+4A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.784+4A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.164+4A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.275+4A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.180+4A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.446+4A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.977+4A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.157+4A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.447+4A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.157+4A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.181+4A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.299+4A>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.280+4A>C
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: n.275+4A>C
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP

17-16343572-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343572
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343572
    reference: chr 17
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.447+5G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.339+5G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.389+5G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.784+5G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.299+5G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.280+5G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.333+5G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.181+5G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.180+5G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.136+5G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.177+5G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.232+5G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.235+5G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.181+5G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.977+5G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.164+5G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.365+5G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.275+5G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.280+5G>A
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: n.275+5G>A
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

17-16343572-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343572
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343572
    reference: chr 17
allele count: 52
allele frequency: 4.286185295087372e-4
allele num: 121320
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.447+5G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.233+5G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.977+5G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.232+5G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.181+5G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.339+5G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.157+5G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.425+5G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.136+5G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.335+5G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.483+5G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.280+5G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.180+5G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.389+5G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.164+5G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.235+5G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.177+5G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.299+5G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.333+5G>C
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: n.275+5G>C
num of homozygotes: 1
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

17-16343578-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343578
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343578
    reference: chr 17
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.389+11C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.425+11C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.447+11C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.339+11C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.333+11C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.233+11C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.136+11C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.365+11C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.977+11C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.180+11C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.157+11C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.177+11C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.447+11C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.181+11C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.275+11C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.235+11C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.232+11C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.157+11C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.280+11C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.280+11C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.164+11C>T
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

17-16343581-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343581
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343581
    reference: chr 17
allele count: 1
allele frequency: 8.246334504312833e-6
allele num: 121266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.339+14T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.447+14T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.299+14T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.235+14T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.164+14T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.177+14T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.597+14T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.483+14T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.335+14T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.136+14T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.446+14T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.425+14T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.389+14T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.280+14T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.181+14T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.232+14T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.180+14T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.447+14T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.181+14T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.784+14T>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.157+14T>A
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

17-16343582-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343582
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343582
    reference: chr 17
allele count: 6
allele frequency: 4.947882306372873e-5
allele num: 121264
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.181+15A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.446+15A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.977+15A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.233+15A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.232+15A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.333+15A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.597+15A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.280+15A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.339+15A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.483+15A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.164+15A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.180+15A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.177+15A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.235+15A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.136+15A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.447+15A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.784+15A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.389+15A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.181+15A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.333+15A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.280+15A>G
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

17-16343596-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343596
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343596
    reference: chr 17
allele count: 1
allele frequency: 8.251097395953662e-6
allele num: 121196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.299+29G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.233+29G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.425+29G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.447+29G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.157+29G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.977+29G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.275+29G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.389+29G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.180+29G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.232+29G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.339+29G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.181+29G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.446+29G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.597+29G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.181+29G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.164+29G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.447+29G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.235+29G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.333+29G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.177+29G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.136+29G>A
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

17-16343602-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343602
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343602
    reference: chr 17
allele count: 1
allele frequency: 8.254639107178234e-6
allele num: 121144
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.232+35C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.597+35C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.977+35C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.333+35C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.275+35C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.335+35C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.389+35C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.447+35C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.280+35C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.784+35C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.164+35C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.177+35C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.447+35C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.280+35C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.339+35C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.299+35C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.180+35C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.181+35C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.235+35C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.157+35C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.333+35C>T
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

17-16343611-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16343611
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16343611
    reference: chr 17
allele count: 3
allele frequency: 2.477536997885835e-5
allele num: 121088
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.447+44G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.333+44G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.181+44G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.425+44G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.180+44G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.447+44G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.280+44G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.232+44G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.177+44G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.164+44G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.335+44G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.784+44G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.389+44G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.299+44G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.233+44G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.235+44G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.483+44G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.446+44G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.339+44G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.597+44G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.280+44G>C
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

17-16344337-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16344337
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16344337
    reference: chr 17
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.336-51T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.598-345T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.236-51T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.785-51T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.447-51T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.181-51T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.158-51T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.340-51T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.426-345T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.233-345T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.390-51T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.448-51T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.234-51T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.165-51T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.281-51T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.181+770T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.178-51T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.978-51T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.366-51T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.333+770T>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.157+770T>C
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

17-16344347-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16344347
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16344347
    reference: chr 17
allele count: 4
allele frequency: 3.294675803900896e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.165-41C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.334-41C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.281-41C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.340-41C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.336-41C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.276-41C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.390-41C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.785-41C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.447-41C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.137-41C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.366-41C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.181-41C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.233-335C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.158-41C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.178-41C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.236-41C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.181+780C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.448-41C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.234-41C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.300-41C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.182-41C>T
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

17-16344349-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16344349
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16344349
    reference: chr 17
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.340-39G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.333+782G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.598-333G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.233-333G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.390-39G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.165-39G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.300-39G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.178-39G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.448-39G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.336-39G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.447-39G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.978-39G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.181-39G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.181+782G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.281-333G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.234-39G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.785-39G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.484-39G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.137-39G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.236-39G>C
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.281-39G>C
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

17-16344350-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16344350
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16344350
    reference: chr 17
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.181-38C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.978-38C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.334-38C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.785-38C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.165-38C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.157+783C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.340-38C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.178-38C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.447-38C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.281-332C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.336-38C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.426-332C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.281-38C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.234-38C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.182-38C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.276-38C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.300-38C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.181+783C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.484-38C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.137-38C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.236-38C>T
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

17-16344357-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16344357
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16344357
    reference: chr 17
allele count: 4
allele frequency: 3.294730079238259e-5
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.366-31T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.448-31T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.340-31T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.281-31T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.426-325T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.234-31T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.182-31T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.137-31T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.281-325T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.598-325T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.300-31T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.236-31T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.333+790T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.233-325T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.178-31T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.165-31T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.978-31T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.390-31T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.448-31T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.276-31T>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.181+790T>G
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

17-16344357-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16344357
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16344358
    reference: chr 17
allele count: 6
allele frequency: 4.942095118857387e-5
allele num: 121406
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.426-323dupA
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.137-29dupA
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.236-29dupA
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.340-29dupA
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.281-29dupA
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.158-29dupA
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.234-29dupA
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.276-29dupA
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.785-29dupA
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.447-29dupA
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.157+792dupA
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.181+792dupA
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.165-29dupA
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.281-323dupA
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.448-29dupA
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.448-29dupA
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.182-29dupA
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.181-29dupA
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.366-29dupA
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.233-323dupA
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.978-29dupA
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 1
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

17-16344361-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16344361
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16344361
    reference: chr 17
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.236-27G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.426-321G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.165-27G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.181+794G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.281-321G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.181-27G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.340-27G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.233-321G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.157+794G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.300-27G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.598-321G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.276-27G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.334-27G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.178-27G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.281-27G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.366-27G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.182-27G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.234-27G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.448-27G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.158-27G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.336-27G>A
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

17-16344365-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16344365
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16344365
    reference: chr 17
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.785-23A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.181+798A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.158-23A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.334-23A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.165-23A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.448-23A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.300-23A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.281-317A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.340-23A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.233-317A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.447-23A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.598-317A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.234-23A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.137-23A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.181-23A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.484-23A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.333+798A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.236-23A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.336-23A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.182-23A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.281-23A>G
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS

17-16344368-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16344368
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16344368
    reference: chr 17
allele count: 19
allele frequency: 1.565022569272841e-4
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.448-20C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.336-20C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.390-20C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.234-20C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.276-20C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.178-20C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.340-20C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.181-20C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.300-20C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.182-20C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.447-20C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.236-20C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.978-20C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.137-20C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.158-20C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.165-20C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.281-20C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.785-20C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.426-314C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.157+801C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.598-314C>T
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

17-16344369-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16344369
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16344369
    reference: chr 17
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.165-19G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.276-19G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.182-19G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.340-19G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.978-19G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.234-19G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.236-19G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.334-19G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.448-19G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.281-19G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.181+802G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.300-19G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.158-19G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.178-19G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.181-19G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.447-19G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.333+802G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.157+802G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.448-19G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.233-313G>A
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.785-19G>A
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

17-16344374-C-CTCCAT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16344374
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16344379
    reference: chr 17
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: CTCCAT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.448-10_448-6dupATTCC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.178-10_178-6dupATTCC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000480811
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000480811.1:n.447-10_447-6dupATTCC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.390-10_390-6dupATTCC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.333+811_333+815dupATTCC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.978-10_978-6dupATTCC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.300-10_300-6dupATTCC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.448-10_448-6dupATTCC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.158-10_158-6dupATTCC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.366-10_366-6dupATTCC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.137-10_137-6dupATTCC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.165-10_165-6dupATTCC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.233-304_233-300dupATTCC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.181-10_181-6dupATTCC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.340-10_340-6dupATTCC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.236-10_236-6dupATTCC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.181+811_181+815dupATTCC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000470491
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000470491.2:n.426-304_426-300dupATTCC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.334-10_334-6dupATTCC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.276-10_276-6dupATTCC
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.785-10_785-6dupATTCC
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD

17-16344376-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16344376
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16344376
    reference: chr 17
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.236-12C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.334-12C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.181+809C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.366-12C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.390-12C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.448-12C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.448-12C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.336-12C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.978-12C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.234-12C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.233-306C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.340-12C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.276-12C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.157+809C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483140
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483140.1:n.281-306C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.181-12C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.785-12C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.182-12C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.165-12C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.598-306C>T
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.158-12C>T
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

17-16344386-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16344386
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16344386
    reference: chr 17
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000492250
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000492250.1:n.137-2A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.334-2A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.181-2A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.236-2A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.484-2A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.178-2A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000484836
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000484836.1:n.390-2A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581913
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581913.1:n.598-296A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000491009
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000491009.1:n.158-2A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.281-2A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.182-2A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.300-2A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.165-2A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.366-2A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.340-2A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.785-2A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581361
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581361.1:n.181+819A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.448-2A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.276-2A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.233-296A>G
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.333+819A>G
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: n.276-2A>G
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

17-16344398-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16344398
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 16344396
    reference: chr 17
allele count: 3
allele frequency: 2.471047559428694e-5
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000581718
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000581718.1:n.461_462delAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584177
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584177.1:n.379_380delAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580770
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580770.1:n.195_196delAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000487066
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000487066.1:n.349_350delAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584926
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584926.1:n.313_314delAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000478103
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000478103.2:n.347_348delAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000579473
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000579473.1:n.194_195delAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000582911
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000582911.1:n.191_192delAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000578757
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000578757.1:n.798_799delAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000497774
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000497774.1:n.991_992delAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000580180
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000580180.1:n.247_248delAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481898
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481898.1:n.289_290delAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000481027
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000481027.1:n.353_354delAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000583400
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000583400.2:n.178_179delAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000483588
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000483588.2:n.157+834_157+835delAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000477249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000477249.2:n.249_250delAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000472367
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000472367.1:n.333+834_333+835delAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000460249
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000460249.1:n.294_295delAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475947
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475947.2:n.233-281_233-280delAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000584141
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000584141.1:n.461_462delAG
  variant of: http://identifiers.org/hgnc/28619
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175061
  ensembl transcript: ENST00000475953
  gene symbol: FAM211A-AS1
  hgvsc: ENST00000475953.1:n.497_498delAG
  variant of: http://identifiers.org/hgnc/28619
canonical: true
consequence: non coding transcript exon
filter: PASS
num of homozygotes: 0
reference allele: CAG

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584141
gene symbol: FAM211A-AS1
hgvsc: ENST00000584141.1:n.379-70delG
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584177
gene symbol: FAM211A-AS1
hgvsc: ENST00000584177.1:n.297-70delG
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000470491
gene symbol: FAM211A-AS1
hgvsc: ENST00000470491.2:n.357-70delG
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.529-70delG
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000492250
gene symbol: FAM211A-AS1
hgvsc: ENST00000492250.1:n.68-70delG
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000472367
gene symbol: FAM211A-AS1
hgvsc: ENST00000472367.1:n.265-70delG
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000578757
gene symbol: FAM211A-AS1
hgvsc: ENST00000578757.1:n.646delG
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000460249
gene symbol: FAM211A-AS1
hgvsc: ENST00000460249.1:n.212-70delG
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 36
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 161
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 470
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 8611
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2070
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14072
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 969
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3407
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 37
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5505
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1457
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 6858
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 61
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 323
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 699
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15575
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2984
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8254
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21444
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12558
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 5376
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3528
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4395
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.422774076317383e-4
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.120000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.628e1

MQ
type: SiteQuality
SIO_000300: 5.981e1

VQSLOD
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 2.140876e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

FS
type: SiteQuality
SIO_000300: 8.765000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.01e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581361
gene symbol: FAM211A-AS1
hgvsc: ENST00000581361.1:n.113-71A>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475953
gene symbol: FAM211A-AS1
hgvsc: ENST00000475953.1:n.415-71A>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000477249
gene symbol: FAM211A-AS1
hgvsc: ENST00000477249.2:n.96A>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475947
gene symbol: FAM211A-AS1
hgvsc: ENST00000475947.2:n.164-71A>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580180
gene symbol: FAM211A-AS1
hgvsc: ENST00000580180.1:n.165-71A>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000470491
gene symbol: FAM211A-AS1
hgvsc: ENST00000470491.2:n.357-71A>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000478103
gene symbol: FAM211A-AS1
hgvsc: ENST00000478103.2:n.265-71A>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000579473
gene symbol: FAM211A-AS1
hgvsc: ENST00000579473.1:n.112-71A>T
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8611
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5505
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 470
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1457
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2070
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15575
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 323
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14072
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 699
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3407
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 161
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 61
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6858
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 969
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21444
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5376
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2984
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8254
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12558
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3528
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4395
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.981e1

QD
type: SiteQuality
SIO_000300: 1.628e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.24e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.120000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.31e0

FS
type: SiteQuality
SIO_000300: 8.765000000000001e0

DP
type: SiteQuality
SIO_000300: 2.140876e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000481027
gene symbol: FAM211A-AS1
hgvsc: ENST00000481027.1:n.271-62_271-60delCAC
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581718
gene symbol: FAM211A-AS1
hgvsc: ENST00000581718.1:n.379-62_379-60delCAC
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000491009
gene symbol: FAM211A-AS1
hgvsc: ENST00000491009.1:n.89-62_89-60delCAC
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000487066
gene symbol: FAM211A-AS1
hgvsc: ENST00000487066.1:n.267-62_267-60delCAC
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000460249
gene symbol: FAM211A-AS1
hgvsc: ENST00000460249.1:n.212-62_212-60delCAC
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475953
gene symbol: FAM211A-AS1
hgvsc: ENST00000475953.1:n.415-62_415-60delCAC
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580770
gene symbol: FAM211A-AS1
hgvsc: ENST00000580770.1:n.113-62_113-60delCAC
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475947
gene symbol: FAM211A-AS1
hgvsc: ENST00000475947.2:n.164-62_164-60delCAC
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 5504
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 161
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 469
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8610
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2070
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6859
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 969
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3406
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 15583
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14070
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 67
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 699
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1456
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 323
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8256
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3530
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4396
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5376
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21444
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2983
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12555
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.605e1

MQRankSum
type: SiteQuality
SIO_000300: -7.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.49e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

FS
type: SiteQuality
SIO_000300: 3.467e0

DP
type: SiteQuality
SIO_000300: 2.140807e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.78e-1

MQ
type: SiteQuality
SIO_000300: 5.588e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.04e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000487066
gene symbol: FAM211A-AS1
hgvsc: ENST00000487066.1:n.267-65C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584926
gene symbol: FAM211A-AS1
hgvsc: ENST00000584926.1:n.166C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000460249
gene symbol: FAM211A-AS1
hgvsc: ENST00000460249.1:n.212-65C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580770
gene symbol: FAM211A-AS1
hgvsc: ENST00000580770.1:n.113-65C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000481898
gene symbol: FAM211A-AS1
hgvsc: ENST00000481898.1:n.207-65C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475953
gene symbol: FAM211A-AS1
hgvsc: ENST00000475953.1:n.415-65C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000582911
gene symbol: FAM211A-AS1
hgvsc: ENST00000582911.1:n.109-65C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475947
gene symbol: FAM211A-AS1
hgvsc: ENST00000475947.2:n.164-65C>T
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 66
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6856
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2071
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1456
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14077
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 469
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3408
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5504
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 35
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 214
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 698
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 113
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 161
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 324
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 8611
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15580
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 969
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4396
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5375
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21432
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3530
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12551
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 8255
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2983
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.996462087368453e-5
allele num: 66706
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.322e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.55e-1

DP
type: SiteQuality
SIO_000300: 2.140999e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

MQRankSum
type: SiteQuality
SIO_000300: -4.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.668e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.648e0

QD
type: SiteQuality
SIO_000300: 1.206e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000492250
gene symbol: FAM211A-AS1
hgvsc: ENST00000492250.1:n.68-57G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580770
gene symbol: FAM211A-AS1
hgvsc: ENST00000580770.1:n.113-57G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000470491
gene symbol: FAM211A-AS1
hgvsc: ENST00000470491.2:n.357-57G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475947
gene symbol: FAM211A-AS1
hgvsc: ENST00000475947.2:n.164-57G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584926
gene symbol: FAM211A-AS1
hgvsc: ENST00000584926.1:n.174G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000480811
gene symbol: FAM211A-AS1
hgvsc: ENST00000480811.1:n.378-57G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000491009
gene symbol: FAM211A-AS1
hgvsc: ENST00000491009.1:n.89-57G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584177
gene symbol: FAM211A-AS1
hgvsc: ENST00000584177.1:n.297-57G>C
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 323
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2070
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5501
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15600
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 969
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 214
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8605
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 162
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 14071
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1456
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 696
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 469
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6854
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 32
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3407
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21461
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2980
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3527
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8261
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12544
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5367
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4396
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.19e-1

QD
type: SiteQuality
SIO_000300: 1.212e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

FS
type: SiteQuality
SIO_000300: 1.483e0

MQRankSum
type: SiteQuality
SIO_000300: -1.006e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.963e0

DP
type: SiteQuality
SIO_000300: 2.140907e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.529-48C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000579473
gene symbol: FAM211A-AS1
hgvsc: ENST00000579473.1:n.112-48C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584141
gene symbol: FAM211A-AS1
hgvsc: ENST00000584141.1:n.379-48C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580770
gene symbol: FAM211A-AS1
hgvsc: ENST00000580770.1:n.113-48C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000487066
gene symbol: FAM211A-AS1
hgvsc: ENST00000487066.1:n.267-48C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000480811
gene symbol: FAM211A-AS1
hgvsc: ENST00000480811.1:n.378-48C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000470491
gene symbol: FAM211A-AS1
hgvsc: ENST00000470491.2:n.357-48C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000583400
gene symbol: FAM211A-AS1
hgvsc: ENST00000583400.2:n.96-48C>T
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 15612
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14076
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 324
bin: 7.75e1
variant carriers: 2

GenotypeDepth
all individuals: 3404
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 698
bin: 6.75e1
variant carriers: 2

GenotypeDepth
all individuals: 8604
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6856
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 968
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 79
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 214
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5496
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1456
bin: 5.75e1
variant carriers: 4

GenotypeDepth
all individuals: 469
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2069
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 162
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21462
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3524
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12533
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8260
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1969
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4398
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2978
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5361
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.348839997602062e-4
allele num: 66724
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.883506343713956e-4
allele num: 10404
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

QD
type: SiteQuality
SIO_000300: 1.479e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.575e0

FS
type: SiteQuality
SIO_000300: 1.128e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.95e-1

DP
type: SiteQuality
SIO_000300: 2.141011e6

MQ
type: SiteQuality
SIO_000300: 5.941e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000487066
gene symbol: FAM211A-AS1
hgvsc: ENST00000487066.1:n.267-47A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.529-47A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000481898
gene symbol: FAM211A-AS1
hgvsc: ENST00000481898.1:n.207-47A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584141
gene symbol: FAM211A-AS1
hgvsc: ENST00000584141.1:n.379-47A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584177
gene symbol: FAM211A-AS1
hgvsc: ENST00000584177.1:n.297-47A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000470491
gene symbol: FAM211A-AS1
hgvsc: ENST00000470491.2:n.357-47A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483588
gene symbol: FAM211A-AS1
hgvsc: ENST00000483588.2:n.89-47A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000583400
gene symbol: FAM211A-AS1
hgvsc: ENST00000583400.2:n.96-47A>G
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 8607
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 695
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14078
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6855
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 967
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 113
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3403
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5497
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15620
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2072
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 214
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1452
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 322
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 469
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4399
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3524
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1969
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2979
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8267
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12524
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5367
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21499
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997332374186974e-5
allele num: 66726
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.140545e6

VQSLOD
type: SiteQuality
SIO_000300: 8.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.69e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

MQRankSum
type: SiteQuality
SIO_000300: -5.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.38e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.01e-1

QD
type: SiteQuality
SIO_000300: 1.13e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581718
gene symbol: FAM211A-AS1
hgvsc: ENST00000581718.1:n.379-44A>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.529-44A>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000480811
gene symbol: FAM211A-AS1
hgvsc: ENST00000480811.1:n.378-44A>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584177
gene symbol: FAM211A-AS1
hgvsc: ENST00000584177.1:n.297-44A>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475947
gene symbol: FAM211A-AS1
hgvsc: ENST00000475947.2:n.164-44A>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000583400
gene symbol: FAM211A-AS1
hgvsc: ENST00000583400.2:n.96-44A>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000492250
gene symbol: FAM211A-AS1
hgvsc: ENST00000492250.1:n.68-44A>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000481898
gene symbol: FAM211A-AS1
hgvsc: ENST00000481898.1:n.207-44A>T
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 214
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 73
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3402
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 695
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8606
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 967
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15621
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14077
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1452
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 322
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2071
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6865
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5495
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 469
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8263
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3521
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4397
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1969
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2979
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12522
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5364
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21516
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.91e-1

FS
type: SiteQuality
SIO_000300: 3.357e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.803e0

DP
type: SiteQuality
SIO_000300: 2.140406e6

QD
type: SiteQuality
SIO_000300: 1.105e1

MQ
type: SiteQuality
SIO_000300: 5.965e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.33e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.78e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000481027
gene symbol: FAM211A-AS1
hgvsc: ENST00000481027.1:n.271-36T>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483140
gene symbol: FAM211A-AS1
hgvsc: ENST00000483140.1:n.212-36T>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000487066
gene symbol: FAM211A-AS1
hgvsc: ENST00000487066.1:n.267-36T>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584926
gene symbol: FAM211A-AS1
hgvsc: ENST00000584926.1:n.195T>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580180
gene symbol: FAM211A-AS1
hgvsc: ENST00000580180.1:n.165-36T>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475947
gene symbol: FAM211A-AS1
hgvsc: ENST00000475947.2:n.164-36T>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000582911
gene symbol: FAM211A-AS1
hgvsc: ENST00000582911.1:n.109-36T>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000491009
gene symbol: FAM211A-AS1
hgvsc: ENST00000491009.1:n.89-36T>G
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 14086
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 57
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 695
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1454
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 8601
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 967
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15628
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 214
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 158
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2071
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 469
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5496
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 322
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3401
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6873
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8261
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2982
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12524
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5360
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4395
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3523
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21539
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1968
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.586e0

MQRankSum
type: SiteQuality
SIO_000300: 5.75e-1

FS
type: SiteQuality
SIO_000300: 7.376e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.48e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.65e-1

DP
type: SiteQuality
SIO_000300: 2.140501e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475953
gene symbol: FAM211A-AS1
hgvsc: ENST00000475953.1:n.415-30A>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000491009
gene symbol: FAM211A-AS1
hgvsc: ENST00000491009.1:n.89-30A>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000478103
gene symbol: FAM211A-AS1
hgvsc: ENST00000478103.2:n.265-30A>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000472367
gene symbol: FAM211A-AS1
hgvsc: ENST00000472367.1:n.265-30A>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000582911
gene symbol: FAM211A-AS1
hgvsc: ENST00000582911.1:n.109-30A>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000484836
gene symbol: FAM211A-AS1
hgvsc: ENST00000484836.1:n.291A>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581718
gene symbol: FAM211A-AS1
hgvsc: ENST00000581718.1:n.379-30A>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000583400
gene symbol: FAM211A-AS1
hgvsc: ENST00000583400.2:n.96-30A>C
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3392
bin: 4.75e1
variant carriers: 8

GenotypeDepth
all individuals: 14070
bin: 3.25e1
variant carriers: 3

GenotypeDepth
all individuals: 1457
bin: 5.75e1
variant carriers: 13

GenotypeDepth
all individuals: 324
bin: 7.75e1
variant carriers: 4

GenotypeDepth
all individuals: 116
bin: 8.75e1
variant carriers: 4

GenotypeDepth
all individuals: 40
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 6872
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 165
bin: 9.75e1
variant carriers: 7

GenotypeDepth
all individuals: 2075
bin: 5.25e1
variant carriers: 11

GenotypeDepth
all individuals: 5494
bin: 4.25e1
variant carriers: 4

GenotypeDepth
all individuals: 15634
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 8599
bin: 3.75e1
variant carriers: 4

GenotypeDepth
all individuals: 698
bin: 6.75e1
variant carriers: 8

GenotypeDepth
all individuals: 221
bin: 8.25e1
variant carriers: 7

GenotypeDepth
all individuals: 71
bin: 9.25e1
variant carriers: 3

GenotypeDepth
all individuals: 971
bin: 6.25e1
variant carriers: 10

GenotypeDepth
all individuals: 477
bin: 7.25e1
variant carriers: 12

GenotypeQuality
all individuals: 5350
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8246
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21577
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4389
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3519
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2979
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12564
bin: 9.75e1
variant carriers: 100

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 99
allele frequency: 5.996365838885524e-3
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.41e0

FS
type: SiteQuality
SIO_000300: 5.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.41e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.74e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.142723e6

QD
type: SiteQuality
SIO_000300: 1.496e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000478103
gene symbol: FAM211A-AS1
hgvsc: ENST00000478103.2:n.265-22C>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000484836
gene symbol: FAM211A-AS1
hgvsc: ENST00000484836.1:n.299C>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581718
gene symbol: FAM211A-AS1
hgvsc: ENST00000581718.1:n.379-22C>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000487066
gene symbol: FAM211A-AS1
hgvsc: ENST00000487066.1:n.267-22C>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.529-22C>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000481027
gene symbol: FAM211A-AS1
hgvsc: ENST00000481027.1:n.271-22C>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483588
gene symbol: FAM211A-AS1
hgvsc: ENST00000483588.2:n.89-22C>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580180
gene symbol: FAM211A-AS1
hgvsc: ENST00000580180.1:n.165-22C>A
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 15697
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14094
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5500
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6873
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8605
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 113
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1445
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 690
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3388
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 216
bin: 8.25e1
variant carriers: 2

GenotypeDepth
all individuals: 467
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 158
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 961
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2066
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12480
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2981
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21660
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8259
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3523
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5361
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4393
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1968
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 3
allele frequency: 3.311258278145695e-3
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.31e-1

DP
type: SiteQuality
SIO_000300: 2.14004e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.884e0

FS
type: SiteQuality
SIO_000300: 3.478e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.16e-2

QD
type: SiteQuality
SIO_000300: 1.251e1

MQRankSum
type: SiteQuality
SIO_000300: -4.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000484836
gene symbol: FAM211A-AS1
hgvsc: ENST00000484836.1:n.305T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000583400
gene symbol: FAM211A-AS1
hgvsc: ENST00000583400.2:n.96-16T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000492250
gene symbol: FAM211A-AS1
hgvsc: ENST00000492250.1:n.68-16T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475953
gene symbol: FAM211A-AS1
hgvsc: ENST00000475953.1:n.415-16T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.529-16T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483588
gene symbol: FAM211A-AS1
hgvsc: ENST00000483588.2:n.89-16T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000579473
gene symbol: FAM211A-AS1
hgvsc: ENST00000579473.1:n.112-16T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483140
gene symbol: FAM211A-AS1
hgvsc: ENST00000483140.1:n.212-16T>A
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 214
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14093
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 466
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15710
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5497
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 690
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 962
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6874
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8605
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 113
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1445
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 158
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2066
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3388
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2981
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21690
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3521
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8259
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5361
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1968
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12478
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4394
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.912e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.33e-1

QD
type: SiteQuality
SIO_000300: 1.194e1

VQSLOD
type: SiteQuality
SIO_000300: -1.78e0

FS
type: SiteQuality
SIO_000300: 5.934e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.285e0

MQRankSum
type: SiteQuality
SIO_000300: 2.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.33e-2

DP
type: SiteQuality
SIO_000300: 2.139963e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000472367
gene symbol: FAM211A-AS1
hgvsc: ENST00000472367.1:n.265-12A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581718
gene symbol: FAM211A-AS1
hgvsc: ENST00000581718.1:n.379-12A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475947
gene symbol: FAM211A-AS1
hgvsc: ENST00000475947.2:n.164-12A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000481027
gene symbol: FAM211A-AS1
hgvsc: ENST00000481027.1:n.271-12A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000582911
gene symbol: FAM211A-AS1
hgvsc: ENST00000582911.1:n.109-12A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483140
gene symbol: FAM211A-AS1
hgvsc: ENST00000483140.1:n.212-12A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000492250
gene symbol: FAM211A-AS1
hgvsc: ENST00000492250.1:n.68-12A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000470491
gene symbol: FAM211A-AS1
hgvsc: ENST00000470491.2:n.357-12A>G
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5497
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1445
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6881
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3389
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14092
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 690
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15714
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8602
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 214
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 960
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 466
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 113
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2066
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8257
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1967
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21708
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12478
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4392
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5357
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2981
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3522
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.431e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.82e0

FS
type: SiteQuality
SIO_000300: 5.353e0

QD
type: SiteQuality
SIO_000300: 1.435e1

DP
type: SiteQuality
SIO_000300: 2.14004e6

VQSLOD
type: SiteQuality
SIO_000300: -3.409e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.41e-2

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000583400
gene symbol: FAM211A-AS1
hgvsc: ENST00000583400.2:n.96-10A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483588
gene symbol: FAM211A-AS1
hgvsc: ENST00000483588.2:n.89-10A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581718
gene symbol: FAM211A-AS1
hgvsc: ENST00000581718.1:n.379-10A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000472367
gene symbol: FAM211A-AS1
hgvsc: ENST00000472367.1:n.265-10A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584177
gene symbol: FAM211A-AS1
hgvsc: ENST00000584177.1:n.297-10A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000460249
gene symbol: FAM211A-AS1
hgvsc: ENST00000460249.1:n.212-10A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580770
gene symbol: FAM211A-AS1
hgvsc: ENST00000580770.1:n.113-10A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000478103
gene symbol: FAM211A-AS1
hgvsc: ENST00000478103.2:n.265-10A>G
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 467
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15714
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8603
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14090
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5498
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6884
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1444
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2064
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3388
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 322
bin: 7.75e1
variant carriers: 2

GenotypeDepth
all individuals: 159
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 690
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 960
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2980
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12480
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1967
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8257
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21713
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4392
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3521
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5357
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997152704930316e-5
allele num: 66730
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.157e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.24e-1

QD
type: SiteQuality
SIO_000300: 1.437e1

MQRankSum
type: SiteQuality
SIO_000300: 1.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.74e0

FS
type: SiteQuality
SIO_000300: 2.562e0

MQ
type: SiteQuality
SIO_000300: 5.999e1

DP
type: SiteQuality
SIO_000300: 2.140075e6

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000481898
gene symbol: FAM211A-AS1
hgvsc: ENST00000481898.1:n.207-8delT
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000460249
gene symbol: FAM211A-AS1
hgvsc: ENST00000460249.1:n.212-8delT
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483140
gene symbol: FAM211A-AS1
hgvsc: ENST00000483140.1:n.212-8delT
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000478103
gene symbol: FAM211A-AS1
hgvsc: ENST00000478103.2:n.265-8delT
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584141
gene symbol: FAM211A-AS1
hgvsc: ENST00000584141.1:n.379-8delT
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000492250
gene symbol: FAM211A-AS1
hgvsc: ENST00000492250.1:n.68-8delT
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000491009
gene symbol: FAM211A-AS1
hgvsc: ENST00000491009.1:n.89-8delT
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000579473
gene symbol: FAM211A-AS1
hgvsc: ENST00000579473.1:n.112-8delT
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 322
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 690
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 15714
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3388
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14090
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1444
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 960
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8603
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5498
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 6884
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 467
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2064
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21713
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2980
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3521
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1967
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5357
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8257
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4392
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12480
bin: 9.75e1
variant carriers: 4

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.422774076317383e-4
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.437e1

MQRankSum
type: SiteQuality
SIO_000300: 1.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.12e-1

DP
type: SiteQuality
SIO_000300: 2.140075e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.562e0

VQSLOD
type: SiteQuality
SIO_000300: 2.74e0

MQ
type: SiteQuality
SIO_000300: 5.999e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.157e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000491009
gene symbol: FAM211A-AS1
hgvsc: ENST00000491009.1:n.90T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000487066
gene symbol: FAM211A-AS1
hgvsc: ENST00000487066.1:n.268T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000477249
gene symbol: FAM211A-AS1
hgvsc: ENST00000477249.2:n.168T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000478103
gene symbol: FAM211A-AS1
hgvsc: ENST00000478103.2:n.266T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584177
gene symbol: FAM211A-AS1
hgvsc: ENST00000584177.1:n.298T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000578757
gene symbol: FAM211A-AS1
hgvsc: ENST00000578757.1:n.717T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000579473
gene symbol: FAM211A-AS1
hgvsc: ENST00000579473.1:n.113T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584141
gene symbol: FAM211A-AS1
hgvsc: ENST00000584141.1:n.380T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000484836
gene symbol: FAM211A-AS1
hgvsc: ENST00000484836.1:n.322T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000481898
gene symbol: FAM211A-AS1
hgvsc: ENST00000481898.1:n.208T>A
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 6889
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 957
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8605
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 214
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1444
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3389
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 690
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15720
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 468
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14092
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2064
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5496
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21728
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4394
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3523
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1967
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12475
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5356
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8254
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2980
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.01e0

DP
type: SiteQuality
SIO_000300: 2.139995e6

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.53e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

MQRankSum
type: SiteQuality
SIO_000300: 1.21e-1

QD
type: SiteQuality
SIO_000300: 1.248e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584926
gene symbol: FAM211A-AS1
hgvsc: ENST00000584926.1:n.232T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000481898
gene symbol: FAM211A-AS1
hgvsc: ENST00000481898.1:n.208T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580770
gene symbol: FAM211A-AS1
hgvsc: ENST00000580770.1:n.114T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000582911
gene symbol: FAM211A-AS1
hgvsc: ENST00000582911.1:n.110T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475947
gene symbol: FAM211A-AS1
hgvsc: ENST00000475947.2:n.165T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000497774
gene symbol: FAM211A-AS1
hgvsc: ENST00000497774.1:n.910T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475953
gene symbol: FAM211A-AS1
hgvsc: ENST00000475953.1:n.416T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000480811
gene symbol: FAM211A-AS1
hgvsc: ENST00000480811.1:n.379T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000491009
gene symbol: FAM211A-AS1
hgvsc: ENST00000491009.1:n.90T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000487066
gene symbol: FAM211A-AS1
hgvsc: ENST00000487066.1:n.268T>C
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 15720
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 214
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 468
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3389
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5496
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1444
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 957
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2064
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 690
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14092
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6889
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8605
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12475
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3523
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4394
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1967
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21728
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8254
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5356
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2980
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.023888720895071e-4
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.248e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.73e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.01e0

MQRankSum
type: SiteQuality
SIO_000300: 1.21e-1

DP
type: SiteQuality
SIO_000300: 2.139995e6

MQ
type: SiteQuality
SIO_000300: 5.982e1

FS
type: SiteQuality
SIO_000300: 1.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000470491
gene symbol: FAM211A-AS1
hgvsc: ENST00000470491.2:n.360G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584177
gene symbol: FAM211A-AS1
hgvsc: ENST00000584177.1:n.300G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584926
gene symbol: FAM211A-AS1
hgvsc: ENST00000584926.1:n.234G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000478103
gene symbol: FAM211A-AS1
hgvsc: ENST00000478103.2:n.268G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.532G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000578757
gene symbol: FAM211A-AS1
hgvsc: ENST00000578757.1:n.719G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000491009
gene symbol: FAM211A-AS1
hgvsc: ENST00000491009.1:n.92G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000472367
gene symbol: FAM211A-AS1
hgvsc: ENST00000472367.1:n.268G>A
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 15721
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 956
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8606
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6892
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1444
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2064
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3389
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14093
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 690
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 113
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 466
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5496
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 214
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 158
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2980
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5355
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1968
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8256
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21729
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3523
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4394
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12472
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.935e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.05e-1

QD
type: SiteQuality
SIO_000300: 1.21e1

VQSLOD
type: SiteQuality
SIO_000300: -8.0e-1

FS
type: SiteQuality
SIO_000300: 9.420999999999999e0

DP
type: SiteQuality
SIO_000300: 2.139922e6

MQRankSum
type: SiteQuality
SIO_000300: -5.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.91e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000478103
gene symbol: FAM211A-AS1
hgvsc: ENST00000478103.2:n.282_287delAATCAG
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000484836
gene symbol: FAM211A-AS1
hgvsc: ENST00000484836.1:n.338_343delAATCAG
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000472367
gene symbol: FAM211A-AS1
hgvsc: ENST00000472367.1:n.282_287delAATCAG
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483588
gene symbol: FAM211A-AS1
hgvsc: ENST00000483588.2:n.106_111delAATCAG
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000481898
gene symbol: FAM211A-AS1
hgvsc: ENST00000481898.1:n.224_229delAATCAG
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.546_551delAATCAG
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000497774
gene symbol: FAM211A-AS1
hgvsc: ENST00000497774.1:n.926_931delAATCAG
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483140
gene symbol: FAM211A-AS1
hgvsc: ENST00000483140.1:n.229_234delAATCAG
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 3389
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 214
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1444
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6887
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15732
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2064
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 466
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 956
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14089
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5496
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8603
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 690
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3522
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1968
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8256
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2980
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4393
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5356
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12470
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21735
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.275e1

MQRankSum
type: SiteQuality
SIO_000300: -5.569e0

QD
type: SiteQuality
SIO_000300: 7.41e0

DP
type: SiteQuality
SIO_000300: 2.139831e6

VQSLOD
type: SiteQuality
SIO_000300: 1.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.4e-2

FS
type: SiteQuality
SIO_000300: 4.054e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.11e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584141
gene symbol: FAM211A-AS1
hgvsc: ENST00000584141.1:n.400A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000478103
gene symbol: FAM211A-AS1
hgvsc: ENST00000478103.2:n.286A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000484836
gene symbol: FAM211A-AS1
hgvsc: ENST00000484836.1:n.342A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000487066
gene symbol: FAM211A-AS1
hgvsc: ENST00000487066.1:n.288A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000470491
gene symbol: FAM211A-AS1
hgvsc: ENST00000470491.2:n.378A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483140
gene symbol: FAM211A-AS1
hgvsc: ENST00000483140.1:n.233A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483588
gene symbol: FAM211A-AS1
hgvsc: ENST00000483588.2:n.110A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000480811
gene symbol: FAM211A-AS1
hgvsc: ENST00000480811.1:n.399A>G
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 14085
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 321
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2064
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1444
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8603
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 955
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 466
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5496
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15735
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3389
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6884
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 690
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 161
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 214
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1968
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21734
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5353
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4392
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2980
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12471
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3523
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8258
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.466605038132656e-4
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.137e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.105e0

QD
type: SiteQuality
SIO_000300: 7.23e0

MQRankSum
type: SiteQuality
SIO_000300: 3.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.25e-1

DP
type: SiteQuality
SIO_000300: 2.139944e6

MQ
type: SiteQuality
SIO_000300: 5.902e1

VQSLOD
type: SiteQuality
SIO_000300: -7.566000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e-2

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000460249
gene symbol: FAM211A-AS1
hgvsc: ENST00000460249.1:n.240T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000481898
gene symbol: FAM211A-AS1
hgvsc: ENST00000481898.1:n.235T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000492250
gene symbol: FAM211A-AS1
hgvsc: ENST00000492250.1:n.96T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475947
gene symbol: FAM211A-AS1
hgvsc: ENST00000475947.2:n.192T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000578757
gene symbol: FAM211A-AS1
hgvsc: ENST00000578757.1:n.744T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000478103
gene symbol: FAM211A-AS1
hgvsc: ENST00000478103.2:n.293T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581361
gene symbol: FAM211A-AS1
hgvsc: ENST00000581361.1:n.141T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581718
gene symbol: FAM211A-AS1
hgvsc: ENST00000581718.1:n.407T>A
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 15737
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 113
bin: 8.75e1
variant carriers: 2

GenotypeDepth
all individuals: 6884
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 466
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 689
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 14084
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8601
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5497
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 160
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1443
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 955
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 321
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2062
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 214
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3390
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4391
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3522
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21740
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1967
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12470
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 2980
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8255
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5353
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.991188635137565e-5
allele num: 66732
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.04e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.86e-1

QD
type: SiteQuality
SIO_000300: 1.292e1

DP
type: SiteQuality
SIO_000300: 2.139855e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.443e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.2e-2

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000582911
gene symbol: FAM211A-AS1
hgvsc: ENST00000582911.1:n.139T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000472367
gene symbol: FAM211A-AS1
hgvsc: ENST00000472367.1:n.295T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.559T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000478103
gene symbol: FAM211A-AS1
hgvsc: ENST00000478103.2:n.295T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584177
gene symbol: FAM211A-AS1
hgvsc: ENST00000584177.1:n.327T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483140
gene symbol: FAM211A-AS1
hgvsc: ENST00000483140.1:n.242T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483588
gene symbol: FAM211A-AS1
hgvsc: ENST00000483588.2:n.119T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000481898
gene symbol: FAM211A-AS1
hgvsc: ENST00000481898.1:n.237T>C
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 6884
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2062
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 955
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5497
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8601
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 214
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14082
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15734
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 692
bin: 6.75e1
variant carriers: 3

GenotypeDepth
all individuals: 163
bin: 9.75e1
variant carriers: 5

GenotypeDepth
all individuals: 466
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3388
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1444
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12472
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8253
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21741
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5351
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2980
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3521
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4391
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 13
allele frequency: 7.874969711654955e-4
allele num: 16508
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.35e-1

FS
type: SiteQuality
SIO_000300: 5.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.13e-1

QD
type: SiteQuality
SIO_000300: 1.288e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.91e0

DP
type: SiteQuality
SIO_000300: 2.13998e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000470491
gene symbol: FAM211A-AS1
hgvsc: ENST00000470491.2:n.388T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483140
gene symbol: FAM211A-AS1
hgvsc: ENST00000483140.1:n.243T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000480811
gene symbol: FAM211A-AS1
hgvsc: ENST00000480811.1:n.409T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581361
gene symbol: FAM211A-AS1
hgvsc: ENST00000581361.1:n.144T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.560T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000481898
gene symbol: FAM211A-AS1
hgvsc: ENST00000481898.1:n.238T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000472367
gene symbol: FAM211A-AS1
hgvsc: ENST00000472367.1:n.296T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000492250
gene symbol: FAM211A-AS1
hgvsc: ENST00000492250.1:n.99T>C
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 159
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 8602
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5497
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3388
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 214
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1441
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2062
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6883
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14087
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 689
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 465
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 956
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 15740
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12462
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3522
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2980
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21747
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4391
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8255
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5352
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997062878379188e-5
allele num: 66732
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.57e0

MQRankSum
type: SiteQuality
SIO_000300: 9.92e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -6.469e-1

QD
type: SiteQuality
SIO_000300: 1.408e1

MQ
type: SiteQuality
SIO_000300: 5.883e1

FS
type: SiteQuality
SIO_000300: 1.958e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.18e0

DP
type: SiteQuality
SIO_000300: 2.13936e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000477249
gene symbol: FAM211A-AS1
hgvsc: ENST00000477249.2:n.211A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000472367
gene symbol: FAM211A-AS1
hgvsc: ENST00000472367.1:n.309A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000491009
gene symbol: FAM211A-AS1
hgvsc: ENST00000491009.1:n.133A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483588
gene symbol: FAM211A-AS1
hgvsc: ENST00000483588.2:n.133A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000478103
gene symbol: FAM211A-AS1
hgvsc: ENST00000478103.2:n.309A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000470491
gene symbol: FAM211A-AS1
hgvsc: ENST00000470491.2:n.401A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.573A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581361
gene symbol: FAM211A-AS1
hgvsc: ENST00000581361.1:n.157A>G
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 14075
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 466
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1441
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8599
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5496
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3387
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15737
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 955
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6877
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 689
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2062
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 158
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 214
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12459
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2980
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8247
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3518
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5348
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4392
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21717
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997242536866083e-5
allele num: 66728
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.227e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.73e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.138928e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

MQRankSum
type: SiteQuality
SIO_000300: 6.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.27e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000579473
gene symbol: FAM211A-AS1
hgvsc: ENST00000579473.1:n.158T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.575T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475953
gene symbol: FAM211A-AS1
hgvsc: ENST00000475953.1:n.461T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584177
gene symbol: FAM211A-AS1
hgvsc: ENST00000584177.1:n.343T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000491009
gene symbol: FAM211A-AS1
hgvsc: ENST00000491009.1:n.135T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000472367
gene symbol: FAM211A-AS1
hgvsc: ENST00000472367.1:n.311T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000578757
gene symbol: FAM211A-AS1
hgvsc: ENST00000578757.1:n.762T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000484836
gene symbol: FAM211A-AS1
hgvsc: ENST00000484836.1:n.367T>C
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 1441
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6876
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5497
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2062
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15740
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8597
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3387
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 688
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14073
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 160
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 319
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 954
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 214
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 465
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5347
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3517
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4392
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8246
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12458
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2980
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21709
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728907330567082e-4
allele num: 11568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.25e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.76e-1

DP
type: SiteQuality
SIO_000300: 2.138841e6

MQRankSum
type: SiteQuality
SIO_000300: 5.21e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.11e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.04e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483140
gene symbol: FAM211A-AS1
hgvsc: ENST00000483140.1:n.259G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483588
gene symbol: FAM211A-AS1
hgvsc: ENST00000483588.2:n.136G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000582911
gene symbol: FAM211A-AS1
hgvsc: ENST00000582911.1:n.156G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584177
gene symbol: FAM211A-AS1
hgvsc: ENST00000584177.1:n.344G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000481898
gene symbol: FAM211A-AS1
hgvsc: ENST00000481898.1:n.254G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581718
gene symbol: FAM211A-AS1
hgvsc: ENST00000581718.1:n.426G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.576G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000484836
gene symbol: FAM211A-AS1
hgvsc: ENST00000484836.1:n.368G>A
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 954
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 6877
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8598
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14070
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5497
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3385
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 214
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 688
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15736
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 465
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2062
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1442
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8244
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3518
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21687
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1964
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4392
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5349
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2979
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12458
bin: 9.75e1
variant carriers: 3

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.496268097479092e-5
allele num: 66722
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.08e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.687e0

VQSLOD
type: SiteQuality
SIO_000300: 9.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.623e0

DP
type: SiteQuality
SIO_000300: 2.138639e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.3e-2

QD
type: SiteQuality
SIO_000300: 1.237e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.22e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580180
gene symbol: FAM211A-AS1
hgvsc: ENST00000580180.1:n.213G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483140
gene symbol: FAM211A-AS1
hgvsc: ENST00000483140.1:n.260G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000472367
gene symbol: FAM211A-AS1
hgvsc: ENST00000472367.1:n.313G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000478103
gene symbol: FAM211A-AS1
hgvsc: ENST00000478103.2:n.313G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000578757
gene symbol: FAM211A-AS1
hgvsc: ENST00000578757.1:n.764G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584177
gene symbol: FAM211A-AS1
hgvsc: ENST00000584177.1:n.345G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584926
gene symbol: FAM211A-AS1
hgvsc: ENST00000584926.1:n.279G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000491009
gene symbol: FAM211A-AS1
hgvsc: ENST00000491009.1:n.137G>A
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5497
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 465
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8598
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1441
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3385
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6877
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2062
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 15738
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 953
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 687
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 214
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14072
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8244
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3519
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5349
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12455
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2979
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4392
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21693
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1964
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

DP
type: SiteQuality
SIO_000300: 2.138547e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 1.06e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.173e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.610000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.24e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483588
gene symbol: FAM211A-AS1
hgvsc: ENST00000483588.2:n.146G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.586G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000470491
gene symbol: FAM211A-AS1
hgvsc: ENST00000470491.2:n.414G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580770
gene symbol: FAM211A-AS1
hgvsc: ENST00000580770.1:n.170G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000491009
gene symbol: FAM211A-AS1
hgvsc: ENST00000491009.1:n.146G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475953
gene symbol: FAM211A-AS1
hgvsc: ENST00000475953.1:n.472G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483140
gene symbol: FAM211A-AS1
hgvsc: ENST00000483140.1:n.269G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000481898
gene symbol: FAM211A-AS1
hgvsc: ENST00000481898.1:n.264G>A
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 3384
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15730
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 953
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1441
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 213
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14063
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 687
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8597
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6892
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2062
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 465
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5496
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21713
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5344
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1962
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2979
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12452
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3516
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4389
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8238
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.59e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.199e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.45e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.055e-1

FS
type: SiteQuality
SIO_000300: 3.394e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.3e-1

DP
type: SiteQuality
SIO_000300: 2.138278e6

MQRankSum
type: SiteQuality
SIO_000300: 1.86e0

MQ
type: SiteQuality
SIO_000300: 5.933e1

QD
type: SiteQuality
SIO_000300: 1.164e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000472367
gene symbol: FAM211A-AS1
hgvsc: ENST00000472367.1:n.329A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000578757
gene symbol: FAM211A-AS1
hgvsc: ENST00000578757.1:n.780A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000497774
gene symbol: FAM211A-AS1
hgvsc: ENST00000497774.1:n.973A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581718
gene symbol: FAM211A-AS1
hgvsc: ENST00000581718.1:n.443A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000460249
gene symbol: FAM211A-AS1
hgvsc: ENST00000460249.1:n.276A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000470491
gene symbol: FAM211A-AS1
hgvsc: ENST00000470491.2:n.421A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000480811
gene symbol: FAM211A-AS1
hgvsc: ENST00000480811.1:n.442A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000478103
gene symbol: FAM211A-AS1
hgvsc: ENST00000478103.2:n.329A>G
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 5494
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14050
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 213
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6887
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 319
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 41
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1441
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8591
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15733
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 158
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2062
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 688
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3382
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 465
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 953
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21721
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2978
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4383
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8239
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3512
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1961
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5345
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12450
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66716
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.019e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.79e-1

QD
type: SiteQuality
SIO_000300: 9.699999999999999e0

DP
type: SiteQuality
SIO_000300: 2.137619e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.99e-2

FS
type: SiteQuality
SIO_000300: 2.233e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584177
gene symbol: FAM211A-AS1
hgvsc: ENST00000584177.1:n.362T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000480811
gene symbol: FAM211A-AS1
hgvsc: ENST00000480811.1:n.443T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483140
gene symbol: FAM211A-AS1
hgvsc: ENST00000483140.1:n.277T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000491009
gene symbol: FAM211A-AS1
hgvsc: ENST00000491009.1:n.154T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580770
gene symbol: FAM211A-AS1
hgvsc: ENST00000580770.1:n.178T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.594T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000497774
gene symbol: FAM211A-AS1
hgvsc: ENST00000497774.1:n.974T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581718
gene symbol: FAM211A-AS1
hgvsc: ENST00000581718.1:n.444T>C
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 14049
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1441
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15727
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3382
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 158
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 213
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 954
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 111
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8592
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 687
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 465
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5494
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2060
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6882
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5347
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8235
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3512
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2979
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1960
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12447
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4383
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21707
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.729206294310911e-4
allele num: 11566
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.36e-2

VQSLOD
type: SiteQuality
SIO_000300: -4.568e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.77e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

DP
type: SiteQuality
SIO_000300: 2.137461e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.271e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.13e0

FS
type: SiteQuality
SIO_000300: 7.198e0

QD
type: SiteQuality
SIO_000300: 1.142e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000491009
gene symbol: FAM211A-AS1
hgvsc: ENST00000491009.1:n.157G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584141
gene symbol: FAM211A-AS1
hgvsc: ENST00000584141.1:n.447G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584177
gene symbol: FAM211A-AS1
hgvsc: ENST00000584177.1:n.365G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581718
gene symbol: FAM211A-AS1
hgvsc: ENST00000581718.1:n.447G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483140
gene symbol: FAM211A-AS1
hgvsc: ENST00000483140.1:n.280G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000478103
gene symbol: FAM211A-AS1
hgvsc: ENST00000478103.2:n.333G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475947
gene symbol: FAM211A-AS1
hgvsc: ENST00000475947.2:n.232G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000492250
gene symbol: FAM211A-AS1
hgvsc: ENST00000492250.1:n.136G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000472367
gene symbol: FAM211A-AS1
hgvsc: ENST00000472367.1:n.333G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000470491
gene symbol: FAM211A-AS1
hgvsc: ENST00000470491.2:n.425G>A
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 213
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3382
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14046
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1442
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5492
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 71
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15711
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 954
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2059
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 685
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8584
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 466
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6870
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2979
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3510
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4382
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8226
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5341
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1960
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21656
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12443
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.77e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.38e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.3e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.382e0

QD
type: SiteQuality
SIO_000300: 1.149e1

DP
type: SiteQuality
SIO_000300: 2.136806e6

MQ
type: SiteQuality
SIO_000300: 5.987e1

VQSLOD
type: SiteQuality
SIO_000300: 5.58e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000497774
gene symbol: FAM211A-AS1
hgvsc: ENST00000497774.1:n.977+3A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.597+3A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000472367
gene symbol: FAM211A-AS1
hgvsc: ENST00000472367.1:n.333+3A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483140
gene symbol: FAM211A-AS1
hgvsc: ENST00000483140.1:n.280+3A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000492250
gene symbol: FAM211A-AS1
hgvsc: ENST00000492250.1:n.136+3A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000470491
gene symbol: FAM211A-AS1
hgvsc: ENST00000470491.2:n.425+3A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000460249
gene symbol: FAM211A-AS1
hgvsc: ENST00000460249.1:n.280+3A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580770
gene symbol: FAM211A-AS1
hgvsc: ENST00000580770.1:n.181+3A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000481898
gene symbol: FAM211A-AS1
hgvsc: ENST00000481898.1:n.275+3A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000491009
gene symbol: FAM211A-AS1
hgvsc: ENST00000491009.1:n.157+3A>G
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 43
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5491
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 954
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 466
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 158
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3381
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 67
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 41
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 15706
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6873
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 79
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14033
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 685
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 213
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1442
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8582
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2061
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1960
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21652
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5338
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3507
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4380
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2979
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8219
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12443
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.062075654704171e-5
allele num: 16496
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.083e1

MQRankSum
type: SiteQuality
SIO_000300: 8.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.473e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.68e0

DP
type: SiteQuality
SIO_000300: 2.136348e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.52e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.206e0

VQSLOD
type: SiteQuality
SIO_000300: 6.0e-2

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000582911
gene symbol: FAM211A-AS1
hgvsc: ENST00000582911.1:n.177+4A>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000492250
gene symbol: FAM211A-AS1
hgvsc: ENST00000492250.1:n.136+4A>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580180
gene symbol: FAM211A-AS1
hgvsc: ENST00000580180.1:n.233+4A>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000472367
gene symbol: FAM211A-AS1
hgvsc: ENST00000472367.1:n.333+4A>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000487066
gene symbol: FAM211A-AS1
hgvsc: ENST00000487066.1:n.335+4A>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000478103
gene symbol: FAM211A-AS1
hgvsc: ENST00000478103.2:n.333+4A>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.597+4A>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000470491
gene symbol: FAM211A-AS1
hgvsc: ENST00000470491.2:n.425+4A>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580770
gene symbol: FAM211A-AS1
hgvsc: ENST00000580770.1:n.181+4A>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000484836
gene symbol: FAM211A-AS1
hgvsc: ENST00000484836.1:n.389+4A>C
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 1442
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8581
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 685
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 321
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5490
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 954
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 41
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2061
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6867
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 466
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14027
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 213
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 158
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3380
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15712
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4379
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8219
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5337
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12443
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2979
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3507
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1959
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21647
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.062075654704171e-5
allele num: 16496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.027e0

FS
type: SiteQuality
SIO_000300: 1.289e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

MQRankSum
type: SiteQuality
SIO_000300: -9.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.54e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.286e-1

QD
type: SiteQuality
SIO_000300: 1.122e1

DP
type: SiteQuality
SIO_000300: 2.136248e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000491009
gene symbol: FAM211A-AS1
hgvsc: ENST00000491009.1:n.157+5G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580180
gene symbol: FAM211A-AS1
hgvsc: ENST00000580180.1:n.233+5G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000480811
gene symbol: FAM211A-AS1
hgvsc: ENST00000480811.1:n.446+5G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.597+5G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475953
gene symbol: FAM211A-AS1
hgvsc: ENST00000475953.1:n.483+5G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581718
gene symbol: FAM211A-AS1
hgvsc: ENST00000581718.1:n.447+5G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483588
gene symbol: FAM211A-AS1
hgvsc: ENST00000483588.2:n.157+5G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000472367
gene symbol: FAM211A-AS1
hgvsc: ENST00000472367.1:n.333+5G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000470491
gene symbol: FAM211A-AS1
hgvsc: ENST00000470491.2:n.425+5G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000487066
gene symbol: FAM211A-AS1
hgvsc: ENST00000487066.1:n.335+5G>A
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 684
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 164
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 93
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5486
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8576
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1441
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 471
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14021
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 957
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15700
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2060
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6867
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3373
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 322
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1955
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21635
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12460
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4375
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3504
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5334
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2975
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8217
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.63e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.45e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.54e-1

QD
type: SiteQuality
SIO_000300: 1.313e1

DP
type: SiteQuality
SIO_000300: 2.136918e6

MQ
type: SiteQuality
SIO_000300: 5.966e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.37e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584141
gene symbol: FAM211A-AS1
hgvsc: ENST00000584141.1:n.447+5G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483588
gene symbol: FAM211A-AS1
hgvsc: ENST00000483588.2:n.157+5G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000472367
gene symbol: FAM211A-AS1
hgvsc: ENST00000472367.1:n.333+5G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584177
gene symbol: FAM211A-AS1
hgvsc: ENST00000584177.1:n.365+5G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.597+5G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000460249
gene symbol: FAM211A-AS1
hgvsc: ENST00000460249.1:n.280+5G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580770
gene symbol: FAM211A-AS1
hgvsc: ENST00000580770.1:n.181+5G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000481898
gene symbol: FAM211A-AS1
hgvsc: ENST00000481898.1:n.275+5G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000578757
gene symbol: FAM211A-AS1
hgvsc: ENST00000578757.1:n.784+5G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000480811
gene symbol: FAM211A-AS1
hgvsc: ENST00000480811.1:n.446+5G>C
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 8576
bin: 3.75e1
variant carriers: 3

GenotypeDepth
all individuals: 14021
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1441
bin: 5.75e1
variant carriers: 6

GenotypeDepth
all individuals: 684
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 322
bin: 7.75e1
variant carriers: 4

GenotypeDepth
all individuals: 15700
bin: 2.75e1
variant carriers: 3

GenotypeDepth
all individuals: 2060
bin: 5.25e1
variant carriers: 4

GenotypeDepth
all individuals: 6867
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 9.25e1
variant carriers: 2

GenotypeDepth
all individuals: 471
bin: 7.25e1
variant carriers: 6

GenotypeDepth
all individuals: 42
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 93
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3373
bin: 4.75e1
variant carriers: 2

GenotypeDepth
all individuals: 957
bin: 6.25e1
variant carriers: 3

GenotypeDepth
all individuals: 5486
bin: 4.25e1
variant carriers: 2

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 4

GenotypeDepth
all individuals: 215
bin: 8.25e1
variant carriers: 3

GenotypeDepth
all individuals: 164
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3504
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4375
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21635
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1955
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5334
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2975
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8217
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12460
bin: 9.75e1
variant carriers: 51

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.062075654704171e-5
allele num: 16496
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 6.733358984224702e-4
allele num: 10396
num of homozygotes: 0

East Asian
type: Population
allele count: 43
allele frequency: 4.969949144706426e-3
allele num: 8652
num of homozygotes: 1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.63e-2

QD
type: SiteQuality
SIO_000300: 1.313e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.45e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.6e-2

DP
type: SiteQuality
SIO_000300: 2.136918e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475953
gene symbol: FAM211A-AS1
hgvsc: ENST00000475953.1:n.483+11C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000472367
gene symbol: FAM211A-AS1
hgvsc: ENST00000472367.1:n.333+11C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.597+11C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580770
gene symbol: FAM211A-AS1
hgvsc: ENST00000580770.1:n.181+11C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000578757
gene symbol: FAM211A-AS1
hgvsc: ENST00000578757.1:n.784+11C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584926
gene symbol: FAM211A-AS1
hgvsc: ENST00000584926.1:n.299+11C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000487066
gene symbol: FAM211A-AS1
hgvsc: ENST00000487066.1:n.335+11C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000480811
gene symbol: FAM211A-AS1
hgvsc: ENST00000480811.1:n.446+11C>T
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 683
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5485
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2058
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 953
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1434
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 15672
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 13997
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 84
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6860
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8576
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3370
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 212
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 157
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 465
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4378
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5330
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3495
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21584
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8201
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1952
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2976
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12415
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499565126113427e-5
allele num: 66686
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.94e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.775e0

FS
type: SiteQuality
SIO_000300: 5.531e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.42e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.74e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.21e0

QD
type: SiteQuality
SIO_000300: 5.71e0

DP
type: SiteQuality
SIO_000300: 2.133226e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000491009
gene symbol: FAM211A-AS1
hgvsc: ENST00000491009.1:n.157+14T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584177
gene symbol: FAM211A-AS1
hgvsc: ENST00000584177.1:n.365+14T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580180
gene symbol: FAM211A-AS1
hgvsc: ENST00000580180.1:n.233+14T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000478103
gene symbol: FAM211A-AS1
hgvsc: ENST00000478103.2:n.333+14T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000481898
gene symbol: FAM211A-AS1
hgvsc: ENST00000481898.1:n.275+14T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483140
gene symbol: FAM211A-AS1
hgvsc: ENST00000483140.1:n.280+14T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000497774
gene symbol: FAM211A-AS1
hgvsc: ENST00000497774.1:n.977+14T>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000472367
gene symbol: FAM211A-AS1
hgvsc: ENST00000472367.1:n.333+14T>A
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 8566
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13966
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3369
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 465
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 211
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 683
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2058
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 953
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 62
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 15629
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1435
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5481
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 212
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 157
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6842
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1952
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12412
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3488
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8185
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5317
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4369
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21520
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2973
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.664009703690868e-5
allele num: 11542
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.073e0

QD
type: SiteQuality
SIO_000300: 9.66e0

FS
type: SiteQuality
SIO_000300: 4.028e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.99e-1

DP
type: SiteQuality
SIO_000300: 2.131432e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000470491
gene symbol: FAM211A-AS1
hgvsc: ENST00000470491.2:n.425+15A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584926
gene symbol: FAM211A-AS1
hgvsc: ENST00000584926.1:n.299+15A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000487066
gene symbol: FAM211A-AS1
hgvsc: ENST00000487066.1:n.335+15A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584141
gene symbol: FAM211A-AS1
hgvsc: ENST00000584141.1:n.447+15A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000481898
gene symbol: FAM211A-AS1
hgvsc: ENST00000481898.1:n.275+15A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483588
gene symbol: FAM211A-AS1
hgvsc: ENST00000483588.2:n.157+15A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584177
gene symbol: FAM211A-AS1
hgvsc: ENST00000584177.1:n.365+15A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000491009
gene symbol: FAM211A-AS1
hgvsc: ENST00000491009.1:n.157+15A>G
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 212
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 318
bin: 7.75e1
variant carriers: 2

GenotypeDepth
all individuals: 15613
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8566
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5478
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 463
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 952
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 225
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 157
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3369
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 683
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13954
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 63
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6836
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 67
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1435
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 138
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2060
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4368
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3485
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8182
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2973
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21490
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1950
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12411
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 5315
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499745043342632e-5
allele num: 66678
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.779010633379565e-4
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.79e-1

QD
type: SiteQuality
SIO_000300: 1.473e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.41e0

DP
type: SiteQuality
SIO_000300: 2.131025e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQ
type: SiteQuality
SIO_000300: 5.958e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000460249
gene symbol: FAM211A-AS1
hgvsc: ENST00000460249.1:n.280+29G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000478103
gene symbol: FAM211A-AS1
hgvsc: ENST00000478103.2:n.333+29G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584177
gene symbol: FAM211A-AS1
hgvsc: ENST00000584177.1:n.365+29G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475953
gene symbol: FAM211A-AS1
hgvsc: ENST00000475953.1:n.483+29G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000578757
gene symbol: FAM211A-AS1
hgvsc: ENST00000578757.1:n.784+29G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483588
gene symbol: FAM211A-AS1
hgvsc: ENST00000483588.2:n.157+29G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483140
gene symbol: FAM211A-AS1
hgvsc: ENST00000483140.1:n.280+29G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000487066
gene symbol: FAM211A-AS1
hgvsc: ENST00000487066.1:n.335+29G>A
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 693
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5464
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15064
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 157
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8516
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 463
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1435
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 13660
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2057
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 952
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 212
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 698
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 683
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3363
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6698
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3430
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4347
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5253
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7977
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2966
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20556
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12399
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1946
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66640
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.070908207867897e-5
allele num: 16472
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.31e-1

QD
type: SiteQuality
SIO_000300: 1.789e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.56e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

DP
type: SiteQuality
SIO_000300: 2.116013e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000491009
gene symbol: FAM211A-AS1
hgvsc: ENST00000491009.1:n.157+35C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584177
gene symbol: FAM211A-AS1
hgvsc: ENST00000584177.1:n.365+35C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000492250
gene symbol: FAM211A-AS1
hgvsc: ENST00000492250.1:n.136+35C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475953
gene symbol: FAM211A-AS1
hgvsc: ENST00000475953.1:n.483+35C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580180
gene symbol: FAM211A-AS1
hgvsc: ENST00000580180.1:n.233+35C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000470491
gene symbol: FAM211A-AS1
hgvsc: ENST00000470491.2:n.425+35C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000480811
gene symbol: FAM211A-AS1
hgvsc: ENST00000480811.1:n.446+35C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580770
gene symbol: FAM211A-AS1
hgvsc: ENST00000580770.1:n.181+35C>T
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 6621
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1417
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 463
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 212
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 881
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 952
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3358
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1435
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14645
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13297
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 157
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5451
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2057
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8469
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 683
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2954
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4319
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19732
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1939
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3375
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7779
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 543
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5193
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12395
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 233
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66614
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.073858114674441e-5
allele num: 16464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.193e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

MQ
type: SiteQuality
SIO_000300: 5.964e1

MQRankSum
type: SiteQuality
SIO_000300: 7.71e-1

DP
type: SiteQuality
SIO_000300: 2.103604e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.799e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581361
gene symbol: FAM211A-AS1
hgvsc: ENST00000581361.1:n.181+44G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483588
gene symbol: FAM211A-AS1
hgvsc: ENST00000483588.2:n.157+44G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000478103
gene symbol: FAM211A-AS1
hgvsc: ENST00000478103.2:n.333+44G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000481898
gene symbol: FAM211A-AS1
hgvsc: ENST00000481898.1:n.275+44G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000491009
gene symbol: FAM211A-AS1
hgvsc: ENST00000491009.1:n.157+44G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000492250
gene symbol: FAM211A-AS1
hgvsc: ENST00000492250.1:n.136+44G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584177
gene symbol: FAM211A-AS1
hgvsc: ENST00000584177.1:n.365+44G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000497774
gene symbol: FAM211A-AS1
hgvsc: ENST00000497774.1:n.977+44G>C
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 7149
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 951
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 463
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 128
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1435
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 683
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3327
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13163
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2057
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3356
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12382
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 157
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5424
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 955
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8357
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 212
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17441
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1927
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7414
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5086
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2949
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1037
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3273
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1388
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1002
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 663
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4280
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12385
bin: 9.75e1
variant carriers: 3

Latino
type: Population
allele count: 3
allele frequency: 2.607335303320007e-4
allele num: 11506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66592
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.074327e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.26e0

QD
type: SiteQuality
SIO_000300: 1.375e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.234e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.04e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584141
gene symbol: FAM211A-AS1
hgvsc: ENST00000584141.1:n.448-51T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000492250
gene symbol: FAM211A-AS1
hgvsc: ENST00000492250.1:n.137-51T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580770
gene symbol: FAM211A-AS1
hgvsc: ENST00000580770.1:n.182-51T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000478103
gene symbol: FAM211A-AS1
hgvsc: ENST00000478103.2:n.334-51T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000481898
gene symbol: FAM211A-AS1
hgvsc: ENST00000481898.1:n.276-51T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475953
gene symbol: FAM211A-AS1
hgvsc: ENST00000475953.1:n.484-51T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483140
gene symbol: FAM211A-AS1
hgvsc: ENST00000483140.1:n.281-345T>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584926
gene symbol: FAM211A-AS1
hgvsc: ENST00000584926.1:n.300-51T>C
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 1375
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2424
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1113
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 47
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1891
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4768
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4787
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 267
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3171
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4367
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 168
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 767
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 357
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30884
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 569
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3735
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 59735
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 152
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.01e-1

DP
type: SiteQuality
SIO_000300: 6.001887e6

FS
type: SiteQuality
SIO_000300: 2.704e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

MQRankSum
type: SiteQuality
SIO_000300: -8.400000000000001e-2

MQ
type: SiteQuality
SIO_000300: 5.94e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

QD
type: SiteQuality
SIO_000300: 1.272e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581718
gene symbol: FAM211A-AS1
hgvsc: ENST00000581718.1:n.448-41C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000472367
gene symbol: FAM211A-AS1
hgvsc: ENST00000472367.1:n.333+780C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000470491
gene symbol: FAM211A-AS1
hgvsc: ENST00000470491.2:n.426-335C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483140
gene symbol: FAM211A-AS1
hgvsc: ENST00000483140.1:n.281-335C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483588
gene symbol: FAM211A-AS1
hgvsc: ENST00000483588.2:n.157+780C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.598-335C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475953
gene symbol: FAM211A-AS1
hgvsc: ENST00000475953.1:n.484-41C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000497774
gene symbol: FAM211A-AS1
hgvsc: ENST00000497774.1:n.978-41C>T
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 1376
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2424
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4768
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 357
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 569
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30883
bin: 9.75e1
variant carriers: 4

GenotypeDepth
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 266
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3735
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 767
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3171
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1112
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1891
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 171
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4787
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4368
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 59735
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.843936190659235e-4
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.138e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.02e0

FS
type: SiteQuality
SIO_000300: 1.199e0

VQSLOD
type: SiteQuality
SIO_000300: 8.42e-1

QD
type: SiteQuality
SIO_000300: 1.3e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

DP
type: SiteQuality
SIO_000300: 6.001927e6

MQ
type: SiteQuality
SIO_000300: 5.952e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483588
gene symbol: FAM211A-AS1
hgvsc: ENST00000483588.2:n.157+782G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000470491
gene symbol: FAM211A-AS1
hgvsc: ENST00000470491.2:n.426-333G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581718
gene symbol: FAM211A-AS1
hgvsc: ENST00000581718.1:n.448-39G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000491009
gene symbol: FAM211A-AS1
hgvsc: ENST00000491009.1:n.158-39G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580770
gene symbol: FAM211A-AS1
hgvsc: ENST00000580770.1:n.182-39G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000478103
gene symbol: FAM211A-AS1
hgvsc: ENST00000478103.2:n.334-39G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000481898
gene symbol: FAM211A-AS1
hgvsc: ENST00000481898.1:n.276-39G>C
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584177
gene symbol: FAM211A-AS1
hgvsc: ENST00000584177.1:n.366-39G>C
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 3736
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 269
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3171
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1376
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 569
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 767
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1891
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 171
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1112
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2424
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4787
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 357
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30882
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 4368
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4768
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59735
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 115
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.443e0

VQSLOD
type: SiteQuality
SIO_000300: -4.579e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.541e1

DP
type: SiteQuality
SIO_000300: 6.001709e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.508e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.95e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.21e0

MQ
type: SiteQuality
SIO_000300: 6.02e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475947
gene symbol: FAM211A-AS1
hgvsc: ENST00000475947.2:n.233-332C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000491009
gene symbol: FAM211A-AS1
hgvsc: ENST00000491009.1:n.158-38C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000472367
gene symbol: FAM211A-AS1
hgvsc: ENST00000472367.1:n.333+783C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.598-332C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000484836
gene symbol: FAM211A-AS1
hgvsc: ENST00000484836.1:n.390-38C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581718
gene symbol: FAM211A-AS1
hgvsc: ENST00000581718.1:n.448-38C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584177
gene symbol: FAM211A-AS1
hgvsc: ENST00000584177.1:n.366-38C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584141
gene symbol: FAM211A-AS1
hgvsc: ENST00000584141.1:n.448-38C>T
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4768
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3171
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4368
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 356
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3736
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 568
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1376
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4788
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30881
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2424
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 268
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 769
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1891
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1112
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 59733
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 175
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.946e1

FS
type: SiteQuality
SIO_000300: 6.794e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.35e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.09e-1

DP
type: SiteQuality
SIO_000300: 6.001631e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.134e0

QD
type: SiteQuality
SIO_000300: 1.328e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.4e-2

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000578757
gene symbol: FAM211A-AS1
hgvsc: ENST00000578757.1:n.785-31T>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475953
gene symbol: FAM211A-AS1
hgvsc: ENST00000475953.1:n.484-31T>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000491009
gene symbol: FAM211A-AS1
hgvsc: ENST00000491009.1:n.158-31T>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000478103
gene symbol: FAM211A-AS1
hgvsc: ENST00000478103.2:n.334-31T>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483588
gene symbol: FAM211A-AS1
hgvsc: ENST00000483588.2:n.157+790T>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000480811
gene symbol: FAM211A-AS1
hgvsc: ENST00000480811.1:n.447-31T>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000487066
gene symbol: FAM211A-AS1
hgvsc: ENST00000487066.1:n.336-31T>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000579473
gene symbol: FAM211A-AS1
hgvsc: ENST00000579473.1:n.181-31T>G
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 1112
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4769
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 569
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 356
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3736
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30880
bin: 9.75e1
variant carriers: 3

GenotypeDepth
all individuals: 4369
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1376
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 768
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 271
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2424
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1890
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3171
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4788
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59733
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 87
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.993766482857828e-5
allele num: 66736
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.24e0

DP
type: SiteQuality
SIO_000300: 6.001825e6

MQ
type: SiteQuality
SIO_000300: 5.987e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.308e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.353e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.22e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.83e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584926
gene symbol: FAM211A-AS1
hgvsc: ENST00000584926.1:n.300-29dupA
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000484836
gene symbol: FAM211A-AS1
hgvsc: ENST00000484836.1:n.390-29dupA
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000487066
gene symbol: FAM211A-AS1
hgvsc: ENST00000487066.1:n.336-29dupA
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000472367
gene symbol: FAM211A-AS1
hgvsc: ENST00000472367.1:n.333+792dupA
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000478103
gene symbol: FAM211A-AS1
hgvsc: ENST00000478103.2:n.334-29dupA
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.598-323dupA
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000582911
gene symbol: FAM211A-AS1
hgvsc: ENST00000582911.1:n.178-29dupA
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475953
gene symbol: FAM211A-AS1
hgvsc: ENST00000475953.1:n.484-29dupA
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1376
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1890
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3736
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1112
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 569
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30880
bin: 9.75e1
variant carriers: 3

GenotypeDepth
all individuals: 4788
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4369
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 356
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4769
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 271
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 768
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3171
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2424
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59733
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 176
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.779010633379565e-4
allele num: 8652
num of homozygotes: 1

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.987e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.83e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.22e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.353e0

QD
type: SiteQuality
SIO_000300: 1.308e1

DP
type: SiteQuality
SIO_000300: 6.001825e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000492250
gene symbol: FAM211A-AS1
hgvsc: ENST00000492250.1:n.137-27G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584141
gene symbol: FAM211A-AS1
hgvsc: ENST00000584141.1:n.448-27G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000578757
gene symbol: FAM211A-AS1
hgvsc: ENST00000578757.1:n.785-27G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000480811
gene symbol: FAM211A-AS1
hgvsc: ENST00000480811.1:n.447-27G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000484836
gene symbol: FAM211A-AS1
hgvsc: ENST00000484836.1:n.390-27G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000472367
gene symbol: FAM211A-AS1
hgvsc: ENST00000472367.1:n.333+794G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475953
gene symbol: FAM211A-AS1
hgvsc: ENST00000475953.1:n.484-27G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000497774
gene symbol: FAM211A-AS1
hgvsc: ENST00000497774.1:n.978-27G>A
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 46
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3737
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4769
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1112
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2424
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 355
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4789
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 270
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 569
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4368
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 175
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30878
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1890
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3172
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 768
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1376
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59731
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.188e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.251e0

DP
type: SiteQuality
SIO_000300: 6.001497e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.119e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.99e-1

FS
type: SiteQuality
SIO_000300: 1.269e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.11e-1

QD
type: SiteQuality
SIO_000300: 1.023e1

Annotation
canonical: true
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000481898
gene symbol: FAM211A-AS1
hgvsc: ENST00000481898.1:n.276-23A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584141
gene symbol: FAM211A-AS1
hgvsc: ENST00000584141.1:n.448-23A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483588
gene symbol: FAM211A-AS1
hgvsc: ENST00000483588.2:n.157+798A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000582911
gene symbol: FAM211A-AS1
hgvsc: ENST00000582911.1:n.178-23A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000484836
gene symbol: FAM211A-AS1
hgvsc: ENST00000484836.1:n.390-23A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000497774
gene symbol: FAM211A-AS1
hgvsc: ENST00000497774.1:n.978-23A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000470491
gene symbol: FAM211A-AS1
hgvsc: ENST00000470491.2:n.426-317A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584177
gene symbol: FAM211A-AS1
hgvsc: ENST00000584177.1:n.366-23A>G
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 355
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3173
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 177
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4368
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4769
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1376
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 768
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 569
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2423
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1112
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 269
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3738
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4789
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30877
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1890
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59732
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 130
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.00146e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.313e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.38e0

QD
type: SiteQuality
SIO_000300: 1.401e1

MQ
type: SiteQuality
SIO_000300: 6.145e1

MQRankSum
type: SiteQuality
SIO_000300: -4.99e-1

FS
type: SiteQuality
SIO_000300: 4.31e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584141
gene symbol: FAM211A-AS1
hgvsc: ENST00000584141.1:n.448-20C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483140
gene symbol: FAM211A-AS1
hgvsc: ENST00000483140.1:n.281-314C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475953
gene symbol: FAM211A-AS1
hgvsc: ENST00000475953.1:n.484-20C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000478103
gene symbol: FAM211A-AS1
hgvsc: ENST00000478103.2:n.334-20C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581361
gene symbol: FAM211A-AS1
hgvsc: ENST00000581361.1:n.181+801C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584177
gene symbol: FAM211A-AS1
hgvsc: ENST00000584177.1:n.366-20C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000472367
gene symbol: FAM211A-AS1
hgvsc: ENST00000472367.1:n.333+801C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475947
gene symbol: FAM211A-AS1
hgvsc: ENST00000475947.2:n.233-314C>T
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 47
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 177
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3172
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1376
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3738
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 357
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30878
bin: 9.75e1
variant carriers: 18

GenotypeDepth
all individuals: 2423
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1890
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 569
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 768
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 266
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4788
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1112
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4769
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4369
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59732
bin: 9.75e1
variant carriers: 19

GenotypeQuality
all individuals: 87
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 2.697275751490994e-4
allele num: 66734
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.002176e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.039e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.01e-1

QD
type: SiteQuality
SIO_000300: 1.211e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.12e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 2.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.93e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483140
gene symbol: FAM211A-AS1
hgvsc: ENST00000483140.1:n.281-313G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000470491
gene symbol: FAM211A-AS1
hgvsc: ENST00000470491.2:n.426-313G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000484836
gene symbol: FAM211A-AS1
hgvsc: ENST00000484836.1:n.390-19G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000487066
gene symbol: FAM211A-AS1
hgvsc: ENST00000487066.1:n.336-19G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584177
gene symbol: FAM211A-AS1
hgvsc: ENST00000584177.1:n.366-19G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.598-313G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475953
gene symbol: FAM211A-AS1
hgvsc: ENST00000475953.1:n.484-19G>A
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000492250
gene symbol: FAM211A-AS1
hgvsc: ENST00000492250.1:n.137-19G>A
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 177
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4771
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1890
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1376
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1113
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 356
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 47
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 569
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2423
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30869
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 768
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 267
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4791
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4368
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3173
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3741
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59731
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 176
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.33e-1

QD
type: SiteQuality
SIO_000300: 1.047e1

MQ
type: SiteQuality
SIO_000300: 5.986e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

DP
type: SiteQuality
SIO_000300: 6.000353e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.59e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580770
gene symbol: FAM211A-AS1
hgvsc: ENST00000580770.1:n.182-10_182-6dupATTCC
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483140
gene symbol: FAM211A-AS1
hgvsc: ENST00000483140.1:n.281-304_281-300dupATTCC
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475953
gene symbol: FAM211A-AS1
hgvsc: ENST00000475953.1:n.484-10_484-6dupATTCC
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483588
gene symbol: FAM211A-AS1
hgvsc: ENST00000483588.2:n.157+811_157+815dupATTCC
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000487066
gene symbol: FAM211A-AS1
hgvsc: ENST00000487066.1:n.336-10_336-6dupATTCC
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000460249
gene symbol: FAM211A-AS1
hgvsc: ENST00000460249.1:n.281-10_281-6dupATTCC
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.598-304_598-300dupATTCC
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580180
gene symbol: FAM211A-AS1
hgvsc: ENST00000580180.1:n.234-10_234-6dupATTCC
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 4771
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1113
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 569
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30868
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 357
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4369
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 267
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1890
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 177
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3741
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3172
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 768
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1376
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4791
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2423
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59731
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.000239e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.49e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.08e0

MQ
type: SiteQuality
SIO_000300: 6.024e1

MQRankSum
type: SiteQuality
SIO_000300: -1.547e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 5.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.39e0

QD
type: SiteQuality
SIO_000300: 1.313e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000460249
gene symbol: FAM211A-AS1
hgvsc: ENST00000460249.1:n.281-12C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000480811
gene symbol: FAM211A-AS1
hgvsc: ENST00000480811.1:n.447-12C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000472367
gene symbol: FAM211A-AS1
hgvsc: ENST00000472367.1:n.333+809C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000475953
gene symbol: FAM211A-AS1
hgvsc: ENST00000475953.1:n.484-12C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000470491
gene symbol: FAM211A-AS1
hgvsc: ENST00000470491.2:n.426-306C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000582911
gene symbol: FAM211A-AS1
hgvsc: ENST00000582911.1:n.178-12C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584926
gene symbol: FAM211A-AS1
hgvsc: ENST00000584926.1:n.300-12C>T
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000492250
gene symbol: FAM211A-AS1
hgvsc: ENST00000492250.1:n.137-12C>T
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 569
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3742
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 267
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 357
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3173
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2423
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 768
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4771
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4791
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4370
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1376
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1888
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30867
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 177
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1113
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59731
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 151
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.53e-1

MQ
type: SiteQuality
SIO_000300: 5.831e1

QD
type: SiteQuality
SIO_000300: 1.255e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.45e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.722e-1

DP
type: SiteQuality
SIO_000300: 6.000213e6

Annotation
canonical: false
consequence: splice_acceptor_variant
consequence: non_coding_transcript_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000480811
gene symbol: FAM211A-AS1
hgvsc: ENST00000480811.1:n.447-2A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: splice_acceptor_variant
consequence: non_coding_transcript_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000580180
gene symbol: FAM211A-AS1
hgvsc: ENST00000580180.1:n.234-2A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483140
gene symbol: FAM211A-AS1
hgvsc: ENST00000483140.1:n.281-296A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: splice_acceptor_variant
consequence: non_coding_transcript_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000584141
gene symbol: FAM211A-AS1
hgvsc: ENST00000584141.1:n.448-2A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000470491
gene symbol: FAM211A-AS1
hgvsc: ENST00000470491.2:n.426-296A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: splice_acceptor_variant
consequence: non_coding_transcript_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000497774
gene symbol: FAM211A-AS1
hgvsc: ENST00000497774.1:n.978-2A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483588
gene symbol: FAM211A-AS1
hgvsc: ENST00000483588.2:n.157+819A>G
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: splice_acceptor_variant
consequence: non_coding_transcript_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000487066
gene symbol: FAM211A-AS1
hgvsc: ENST00000487066.1:n.336-2A>G
variant of: http://identifiers.org/hgnc/28619

GenotypeDepth
all individuals: 46
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3742
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4791
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 357
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 177
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 267
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 569
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3172
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1888
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1113
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4370
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30866
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1376
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 768
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2423
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4772
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 59731
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 124
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.000152e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.284e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.167e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-2

FS
type: SiteQuality
SIO_000300: 2.351e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.41e-1

QD
type: SiteQuality
SIO_000300: 1.264e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000492250
gene symbol: FAM211A-AS1
hgvsc: ENST00000492250.1:n.150_151delAG
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000581913
gene symbol: FAM211A-AS1
hgvsc: ENST00000581913.1:n.598-281_598-280delAG
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000483140
gene symbol: FAM211A-AS1
hgvsc: ENST00000483140.1:n.281-281_281-280delAG
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000470491
gene symbol: FAM211A-AS1
hgvsc: ENST00000470491.2:n.426-281_426-280delAG
variant of: http://identifiers.org/hgnc/28619

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000175061
ensembl transcript: ENST00000484836
gene symbol: FAM211A-AS1
hgvsc: ENST00000484836.1:n.403_404delAG
variant of: http://identifiers.org/hgnc/28619