4-1066917-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1066917
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1066917
    reference: chr 4
allele count: 5
allele frequency: 4.118887570844866e-5
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+470C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*302C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+470C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+470C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+470C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.639C>T
  hgvsp: ENST00000433731.2:c.639C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*316C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+470C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.586C>T
  hgvsp: ENSP00000372428.5:p.Arg196Trp
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*119C>T
  variant of: http://identifiers.org/hgnc/27729
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11405
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg196Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

4-1066920-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1066920
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1066920
    reference: chr 4
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+467G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.636G>A
  hgvsp: ENST00000433731.2:c.636G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*299G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.583G>A
  hgvsp: ENSP00000372428.5:p.Ala195Thr
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+467G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+467G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+467G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*116G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+467G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*313G>A
  variant of: http://identifiers.org/hgnc/27729
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44477
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11414
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3131
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala195Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/4-1066922-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1066922
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1066922
    reference: chr 4
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.634G>T
  hgvsp: ENSP00000389709.2:p.Val212Leu
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*297G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+465G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+465G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+465G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.581G>T
  hgvsp: ENSP00000372428.5:p.Cys194Phe
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*311G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+465G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+465G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*114G>T
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11412
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3131
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val212Leu
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

4-1066927-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1066927
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1066927
    reference: chr 4
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+460C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+460C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*306C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.576C>T
  hgvsp: ENST00000382968.5:c.576C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+460C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.629C>T
  hgvsp: ENSP00000389709.2:p.Pro210Leu
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+460C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*292C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*109C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+460C>T
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro210Leu
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/4-1066935-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1066935
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1066935
    reference: chr 4
allele count: 8
allele frequency: 6.592827004219409e-5
allele num: 121344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+452G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.621G>T
  hgvsp: ENSP00000389709.2:p.Leu207Phe
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+452G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+452G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*305-7G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+452G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+452G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*291-7G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*101G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.575-7G>T
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44396
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11417
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu207Phe
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

4-1066935-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1066935
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1066935
    reference: chr 4
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.575-7G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*291-7G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*305-7G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+452G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*101G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.621G>A
  hgvsp: ENST00000433731.2:c.621G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+452G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+452G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+452G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+452G>A
  variant of: http://identifiers.org/hgnc/27729
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11417
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44396
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
hgvs: c.575-7G>A
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: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD

4-1066939-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1066939
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1066939
    reference: chr 4
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.617C>T
  hgvsp: ENSP00000389709.2:p.Thr206Ile
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+448C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+448C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+448C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*305-11C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*291-11C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*97C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.575-11C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+448C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+448C>T
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44375
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11409
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1281
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr206Ile
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP

4-1066940-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1066940
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1066940
    reference: chr 4
allele count: 5
allele frequency: 4.1209244057627e-5
allele num: 121332
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*305-12A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.616A>G
  hgvsp: ENSP00000389709.2:p.Thr206Ala
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*96A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.575-12A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*291-12A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+447A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+447A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+447A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+447A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+447A>G
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44373
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11408
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr206Ala
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

4-1066940-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1066940
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1066940
    reference: chr 4
allele count: 8
allele frequency: 6.593479049220321e-5
allele num: 121332
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*291-12A>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+447A>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.616A>C
  hgvsp: ENSP00000389709.2:p.Thr206Pro
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*96A>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*305-12A>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+447A>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+447A>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+447A>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.575-12A>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+447A>C
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44373
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11408
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr206Pro
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

4-1066942-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1066942
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1066942
    reference: chr 4
allele count: 3
allele frequency: 2.472676920033628e-5
allele num: 121326
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+445T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.575-14T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*94T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.614T>C
  hgvsp: ENSP00000389709.2:p.Leu205Ser
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+445T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*305-14T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*291-14T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+445T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+445T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+445T>C
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu205Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

4-1066948-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1066948
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1066948
    reference: chr 4
allele count: 1
allele frequency: 8.244702778464837e-6
allele num: 121290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*291-20C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+439C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+439C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+439C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+439C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+439C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.608C>T
  hgvsp: ENSP00000389709.2:p.Pro203Leu
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*88C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*305-20C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.575-20C>T
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1085
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro203Leu
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

4-1066949-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1066949
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1066949
    reference: chr 4
allele count: 1
allele frequency: 8.24551856066228e-6
allele num: 121278
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+438C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*305-21C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+438C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+438C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+438C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*87C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.575-21C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*291-21C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+438C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.607C>T
  hgvsp: ENSP00000389709.2:p.Pro203Ser
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44291
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11412
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro203Ser
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

4-1066954-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1066954
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1066954
    reference: chr 4
allele count: 1
allele frequency: 8.249463784853985e-6
allele num: 121220
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+433T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*291-26T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*82T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+433T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.602T>C
  hgvsp: ENSP00000389709.2:p.Phe201Ser
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*305-26T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+433T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+433T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.575-26T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+433T>C
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11427
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Phe201Ser
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/4-1066958-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1066958
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1066958
    reference: chr 4
allele count: 23
allele frequency: 1.897752401069342e-4
allele num: 121196
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+429T>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+429T>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*305-30T>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+429T>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.575-30T>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+429T>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.598T>G
  hgvsp: ENSP00000389709.2:p.Cys200Gly
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*78T>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*291-30T>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+429T>G
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11421
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 44145
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Cys200Gly
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP

4-1066985-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1066985
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1066985
    reference: chr 4
allele count: 3
allele frequency: 2.502126807786619e-5
allele num: 119898
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.575-4G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+402G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+402G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*55-4G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*291-57G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.575-57G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+402G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+402G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*305-57G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+402G>A
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10962
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
hgvs: c.575-4G>A
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

4-1066986-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1066986
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1066986
    reference: chr 4
allele count: 3
allele frequency: 2.502001601281025e-5
allele num: 119904
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.575-58C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+401C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*55-5C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+401C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*291-58C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+401C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*305-58C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.575-5C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+401C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+401C>T
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11042
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1088
  bin: 9.75e1
  variant carriers: 3
hgvs: c.575-5C>T
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD

4-1066986-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1066986
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1066986
    reference: chr 4
allele count: 3
allele frequency: 2.502001601281025e-5
allele num: 119904
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+401C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*305-58C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*55-5C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+401C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.575-5C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*291-58C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.575-58C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+401C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+401C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+401C>G
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11042
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1036
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 2.75e1
  variant carriers: 0
hgvs: c.575-5C>G
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

4-1066995-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1066995
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1066995
    reference: chr 4
allele count: 1
allele frequency: 8.39898540256337e-6
allele num: 119062
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*55-14G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*291-67G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+392G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+392G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+392G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+392G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.575-67G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+392G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.575-14G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*305-67G>A
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10346
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38269
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3326
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1008
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP

4-1067001-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067001
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067001
    reference: chr 4
allele count: 1
allele frequency: 8.41864224137931e-6
allele num: 118784
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+386T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.575-20T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+386T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+386T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+386T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.575-73T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*55-20T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*305-73T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*291-73T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+386T>C
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3218
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36696
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5495
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3937
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41206
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

4-1067003-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067003
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067004
    reference: chr 4
allele count: 1
allele frequency: 8.427865895797866e-6
allele num: 118654
alternate allele: AT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.575-23_575-22insA
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+383_*353+384insA
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.575-76_575-75insA
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+383_501+384insA
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+383_501+384insA
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+383_147+384insA
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*291-76_*291-75insA
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*55-23_*55-22insA
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*305-76_*305-75insA
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+383_156+384insA
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5981
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35935
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4120
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1079
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

4-1067004-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067004
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067004
    reference: chr 4
allele count: 1
allele frequency: 8.432840855427377e-6
allele num: 118584
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*291-76C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*55-23C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+383C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+383C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*305-76C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.575-23C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+383C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.575-76C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+383C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+383C>A
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35481
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2552
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9343
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39329
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4340
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

4-1067006-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067006
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067006
    reference: chr 4
allele count: 58
allele frequency: 4.900635392726782e-4
allele num: 118352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+381C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.575-78C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.575-25C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+381C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+381C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*55-25C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*305-78C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*291-78C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+381C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+381C>T
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34314
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4978
  bin: 1.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6674
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9189
  bin: 2.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3014
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD

4-1067007-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067007
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067007
    reference: chr 4
allele count: 1
allele frequency: 8.457231778894133e-6
allele num: 118242
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*305-79A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.575-26A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*291-79A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+380A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+380A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+380A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+380A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*55-26A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.575-79A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+380A>G
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6284
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7105
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8915
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2359
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

4-1067011-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067011
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067011
    reference: chr 4
allele count: 2
allele frequency: 1.695346274476562e-5
allele num: 117970
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+376C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.575-30C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*305-83C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.575-83C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+376C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+376C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*291-83C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+376C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*55-30C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+376C>T
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32052
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7043
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2420
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7306
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

4-1067013-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067013
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067013
    reference: chr 4
allele count: 1
allele frequency: 8.498631720293032e-6
allele num: 117666
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.575-32C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*305-85C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+374C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+374C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*55-32C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*291-85C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+374C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.575-85C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+374C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+374C>G
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7511
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2392
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8764
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 765
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

4-1067015-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067015
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067015
    reference: chr 4
allele count: 2
allele frequency: 1.701664227614607e-5
allele num: 117532
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.575-87C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*305-87C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+372C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+372C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*55-34C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*291-87C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+372C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.575-34C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+372C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+372C>T
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7567
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9899
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29534
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3942
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 757
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ

4-1067024-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067024
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067024
    reference: chr 4
allele count: 19
allele frequency: 1.636238374095763e-4
allele num: 116120
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+363A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*291-96A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+363A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*55-43A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.575-96A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+363A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+363A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*305-96A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+363A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.575-43A>G
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7155
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7579
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27811
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 11997
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 990
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

4-1067336-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067336
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067336
    reference: chr 4
allele count: 1
allele frequency: 8.30357884248111e-6
allele num: 120430
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+51G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+51G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*290+51G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+51G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*304+51G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.574+51G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+51G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*54+51G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+51G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.574+51G>A
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7642
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8380
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2949
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14195
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19191
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6896
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3726
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/4-1067342-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067342
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067342
    reference: chr 4
allele count: 1
allele frequency: 8.291461452995706e-6
allele num: 120606
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*54+45T>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+45T>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+45T>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*290+45T>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+45T>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.574+45T>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+45T>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+45T>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*304+45T>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.574+45T>G
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16644
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8364
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4992
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

4-1067345-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067345
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067345
    reference: chr 4
allele count: 2
allele frequency: 1.65898005905969e-5
allele num: 120556
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+42G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*290+42G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.574+42G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+42G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.574+42G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+42G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*304+42G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+42G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+42G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*54+42G>A
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19770
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3656
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1640
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum

4-1067346-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067346
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067346
    reference: chr 4
allele count: 1
allele frequency: 8.292561572269675e-6
allele num: 120590
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*290+41C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+41C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*54+41C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+41C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+41C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+41C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*304+41C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.574+41C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.574+41C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+41C>T
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8523
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18430
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19977
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2333
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-1067349-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067349
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067349
    reference: chr 4
allele count: 1
allele frequency: 8.287201246395068e-6
allele num: 120668
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.574+38C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*54+38C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+38C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+38C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*304+38C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+38C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+38C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+38C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*290+38C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.574+38C>A
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2949
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19435
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1134
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35655
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

4-1067352-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067352
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067352
    reference: chr 4
allele count: 13
allele frequency: 1.076675887429395e-4
allele num: 120742
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+35A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+35A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+35A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+35A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*54+35A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*290+35A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.574+35A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.574+35A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*304+35A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+35A>G
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20554
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20170
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8535
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2947
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 1
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

4-1067357-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067357
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067357
    reference: chr 4
allele count: 5
allele frequency: 4.139826789647121e-5
allele num: 120778
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+30G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+30G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+30G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*54+30G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*290+30G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*304+30G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+30G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.574+30G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+30G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.574+30G>A
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8662
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20636
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2321
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1056
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

4-1067358-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067358
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067358
    reference: chr 4
allele count: 9
allele frequency: 7.450824557917744e-5
allele num: 120792
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+29C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+29C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.574+29C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*54+29C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+29C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+29C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*304+29C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*290+29C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.574+29C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+29C>T
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21076
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20811
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8697
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5316
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

4-1067377-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067377
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067377
    reference: chr 4
allele count: 5
allele frequency: 4.126978886376017e-5
allele num: 121154
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*353+10A>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.156+10A>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.574+10A>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.501+10A>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.574+10A>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*290+10A>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*304+10A>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.147+10A>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*54+10A>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.501+10A>T
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8731
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21789
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

4-1067392-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067392
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067392
    reference: chr 4
allele count: 3
allele frequency: 2.474553343121567e-5
allele num: 121234
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*299G>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*285G>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.142G>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.496G>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.569G>C
  hgvsp: ENSP00000389709.2:p.Arg190Pro
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*348G>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.496G>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.569G>C
  hgvsp: ENSP00000372428.5:p.Arg190Pro
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*49G>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.151G>C
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5314
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg190Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

4-1067392-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067392
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067392
    reference: chr 4
allele count: 2
allele frequency: 1.649702228747711e-5
allele num: 121234
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*285G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.142G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*348G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.569G>A
  hgvsp: ENSP00000389709.2:p.Arg190Gln
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.496G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.569G>A
  hgvsp: ENSP00000372428.5:p.Arg190Gln
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*299G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.496G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*49G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.151G>A
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg190Gln
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD

4-1067393-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067393
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067393
    reference: chr 4
allele count: 1
allele frequency: 8.24783082049421e-6
allele num: 121244
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.568C>T
  hgvsp: ENSP00000389709.2:p.Arg190Ter
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*298C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.495C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.495C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.568C>T
  hgvsp: ENSP00000372428.5:p.Arg190Ter
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.141C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.150C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*48C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*284C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*347C>T
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22017
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg190Ter
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ

4-1067397-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067397
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067397
    reference: chr 4
allele count: 1
allele frequency: 8.246334504312833e-6
allele num: 121266
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.564T>C
  hgvsp: ENST00000433731.2:c.564T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*280T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*44T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.564T>C
  hgvsp: ENST00000382968.5:c.564T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*294T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.491T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.491T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*343T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.146T>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.137T>C
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2947
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22090
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8780
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5310
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp188Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

4-1067398-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067398
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067398
    reference: chr 4
allele count: 1
allele frequency: 8.246470510621453e-6
allele num: 121264
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*293A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.563A>G
  hgvsp: ENSP00000372428.5:p.Asp188Gly
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.563A>G
  hgvsp: ENSP00000389709.2:p.Asp188Gly
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*279A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.136A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*342A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*43A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.490A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.490A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.145A>G
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22088
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2947
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8777
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp188Gly
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff

4-1067400-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067400
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067400
    reference: chr 4
allele count: 2
allele frequency: 1.649158104787506e-5
allele num: 121274
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.561A>C
  hgvsp: ENSP00000389709.2:p.Gln187His
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*277A>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.143A>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*41A>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*340A>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.134A>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*291A>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.488A>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.561A>C
  hgvsp: ENSP00000372428.5:p.Gln187His
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.488A>C
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2947
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gln187His
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

4-1067410-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067410
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067410
    reference: chr 4
allele count: 1
allele frequency: 8.246062505153789e-6
allele num: 121270
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*31G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.478G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*281G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.551G>A
  hgvsp: ENSP00000389709.2:p.Ser184Asn
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.124G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*330G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.551G>A
  hgvsp: ENSP00000372428.5:p.Ser184Asn
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*267G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.133G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.478G>A
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8775
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5311
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser184Asn
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

4-1067427-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067427
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067427
    reference: chr 4
allele count: 36
allele frequency: 2.970346045314279e-4
allele num: 121198
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.534G>A
  hgvsp: ENST00000433731.2:c.534G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.461G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*264G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.461G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*14G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.107G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*250G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*313G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.116G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.534G>A
  hgvsp: ENST00000382968.5:c.534G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22256
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8787
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2104
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala178Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff

4-1067428-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067428
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067428
    reference: chr 4
allele count: 2
allele frequency: 1.650382888830209e-5
allele num: 121184
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.115C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.460C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.460C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.533C>T
  hgvsp: ENSP00000389709.2:p.Ala178Val
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*13C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.533C>T
  hgvsp: ENSP00000372428.5:p.Ala178Val
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*249C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*263C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*312C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.106C>T
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2948
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22286
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala178Val
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

4-1067432-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067432
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067432
    reference: chr 4
allele count: 26
allele frequency: 2.146064447966191e-4
allele num: 121152
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.456C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.102C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.529C>G
  hgvsp: ENSP00000389709.2:p.Pro177Ala
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.529C>G
  hgvsp: ENSP00000372428.5:p.Pro177Ala
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*245C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*259C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*308C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.456C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*9C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.111C>G
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2946
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 22311
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20711
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8787
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro177Ala
num of homozygotes: 1
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

4-1067435-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067435
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067435
    reference: chr 4
allele count: 4
allele frequency: 3.303273544082185e-5
allele num: 121092
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.453G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.99G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*256G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.453G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*242G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*6G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.526G>A
  hgvsp: ENSP00000372428.5:p.Gly176Ser
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.526G>A
  hgvsp: ENSP00000389709.2:p.Gly176Ser
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.108G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*305G>A
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly176Ser
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

4-1067436-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067436
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067436
    reference: chr 4
allele count: 2
allele frequency: 1.651609493451368e-5
allele num: 121094
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.525C>T
  hgvsp: ENST00000433731.2:c.525C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.452C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.525C>T
  hgvsp: ENST00000382968.5:c.525C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.98C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.*5C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*241C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*304C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.452C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.107C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*255C>T
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22323
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala175Ala
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

4-1067455-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067455
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067455
    reference: chr 4
allele count: 1
allele frequency: 8.286651861182008e-6
allele num: 120676
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.438-5C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*227-5C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.511-5C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.438-5C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.511-5C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*241-5C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.84-5C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*290-5C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.88C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.363-5C>A
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22196
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8729
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.511-5C>A
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

4-1067459-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067459
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067459
    reference: chr 4
allele count: 2
allele frequency: 1.659751037344398e-5
allele num: 120500
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*227-9C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*241-9C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.363-9C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.84-9C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*290-9C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.511-9C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.511-9C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.84C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.438-9C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.438-9C>T
  variant of: http://identifiers.org/hgnc/27729
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18893
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6911
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2243
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD

4-1067466-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067466
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067466
    reference: chr 4
allele count: 1
allele frequency: 8.32639467110741e-6
allele num: 120100
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.438-16C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.438-16C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.84-16C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.77C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.511-16C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.363-16C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*241-16C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*227-16C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.511-16C>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*290-16C>G
  variant of: http://identifiers.org/hgnc/27729
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21646
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17435
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8666
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1044
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2243
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS

4-1067471-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067471
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067471
    reference: chr 4
allele count: 2
allele frequency: 1.668056713928273e-5
allele num: 119900
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.363-21G>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.438-21G>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*290-21G>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.84-21G>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.438-21G>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.511-21G>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.72G>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*241-21G>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.511-21G>C
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*227-21G>C
  variant of: http://identifiers.org/hgnc/27729
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16450
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

http://identifiers.org/exac.variant/4-1067471-CAA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067471
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067469
    reference: chr 4
allele count: 2
allele frequency: 1.668056713928273e-5
allele num: 119900
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*290-23_*290-22delTT
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.70_71delTT
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.511-23_511-22delTT
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*241-23_*241-22delTT
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.84-23_84-22delTT
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.438-23_438-22delTT
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.511-23_511-22delTT
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.363-23_363-22delTT
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.438-23_438-22delTT
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*227-23_*227-22delTT
  variant of: http://identifiers.org/hgnc/27729
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1424
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: CAA
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum

4-1067483-TTCCAATATTGCGGCTTACGAGATTCGG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067483
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067456
    reference: chr 4
allele count: 1
allele frequency: 8.370862701109976e-6
allele num: 119462
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  variant of: http://identifiers.org/hgnc/27729
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8067
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7935
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2904
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1771
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 783
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: TTCCAATATTGCGGCTTACGAGATTCGG
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

4-1067486-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067486
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067486
    reference: chr 4
allele count: 1
allele frequency: 8.389120987902887e-6
allele num: 119202
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.511-36G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.511-36G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.84-36G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*227-36G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.438-36G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*290-36G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*241-36G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.57G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.363-36G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.438-36G>A
  variant of: http://identifiers.org/hgnc/27729
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9487
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16029
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8735
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5312
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP

4-1067489-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067489
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067489
    reference: chr 4
allele count: 1
allele frequency: 8.421761832575375e-6
allele num: 118740
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.438-39A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.84-39A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*290-39A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.511-39A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.54A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.363-39A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*227-39A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*241-39A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.438-39A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.511-39A>G
  variant of: http://identifiers.org/hgnc/27729
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14335
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12939
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8461
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8840
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6752
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6121
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2585
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum

4-1067492-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067492
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067492
    reference: chr 4
allele count: 2
allele frequency: 1.685573179159573e-5
allele num: 118654
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*290-42A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.84-42A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.438-42A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.51A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*227-42A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.438-42A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*241-42A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.511-42A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.511-42A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.363-42A>G
  variant of: http://identifiers.org/hgnc/27729
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6359
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2758
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8830
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14964
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15956
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6252
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ

http://identifiers.org/exac.variant/4-1067494-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067494
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067494
    reference: chr 4
allele count: 1
allele frequency: 8.499643014993371e-6
allele num: 117652
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.511-44G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.49G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*227-44G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.363-44G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.84-44G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.511-44G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.438-44G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*241-44G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*290-44G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.438-44G>T
  variant of: http://identifiers.org/hgnc/27729
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8774
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10970
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10519
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14969
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5965
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6372
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6629
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum

4-1067494-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067494
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067494
    reference: chr 4
allele count: 72
allele frequency: 6.119742970795227e-4
allele num: 117652
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.438-44G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.511-44G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.84-44G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.49G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.363-44G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.438-44G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*227-44G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*241-44G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*290-44G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.511-44G>A
  variant of: http://identifiers.org/hgnc/27729
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10519
  bin: 2.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14969
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10970
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5965
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8774
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3851
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5343
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1022
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum

4-1067495-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067495
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067495
    reference: chr 4
allele count: 29
allele frequency: 2.457710430862063e-4
allele num: 117996
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.511-45C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*241-45C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.48C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.511-45C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.363-45C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.438-45C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*227-45C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.84-45C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*290-45C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.438-45C>T
  variant of: http://identifiers.org/hgnc/27729
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11204
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 10578
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14851
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2688
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8868
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4201
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6455
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5353
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP

4-1067501-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067501
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067501
    reference: chr 4
allele count: 11
allele frequency: 9.475407011801188e-5
allele num: 116090
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*290-51G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.84-51G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*227-51G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.363-51G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.42G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.511-51G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*241-51G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.438-51G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.511-51G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.438-51G>A
  variant of: http://identifiers.org/hgnc/27729
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13962
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8809
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4715
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14654
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8741
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1453
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5289
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 1846
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum

4-1067502-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1067502
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1067502
    reference: chr 4
allele count: 1
allele frequency: 8.617420978249629e-6
allele num: 116044
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*290-52C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.438-52C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.511-52C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*227-52C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000508633
  gene symbol: RNF212
  hgvsc: ENST00000508633.1:n.41C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*241-52C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.363-52C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.438-52C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.84-52C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.511-52C>T
  variant of: http://identifiers.org/hgnc/27729
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8785
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14618
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8850
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4683
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4426
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 668
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

4-1073382-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1073382
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1073382
    reference: chr 4
allele count: 2
allele frequency: 1.654287084980728e-5
allele num: 120898
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*227-5932A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.437+49A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.437+49A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*289+49A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.83+49A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.510+49A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*240+49A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.363-5932A>G
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.510+49A>G
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5674
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2494
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10998
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5798
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25777
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ

4-1073387-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1073387
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1073387
    reference: chr 4
allele count: 2
allele frequency: 1.654314452091054e-5
allele num: 120896
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.437+44G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.510+44G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.83+44G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.437+44G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.510+44G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*289+44G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*240+44G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*227-5937G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.363-5937G>A
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10988
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9620
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2494
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9319
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4587
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2387
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD

4-1073389-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1073389
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1073389
    reference: chr 4
allele count: 2
allele frequency: 1.654423929587718e-5
allele num: 120888
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.437+42G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*227-5939G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.363-5939G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*289+42G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.83+42G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.437+42G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.510+42G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.510+42G>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*240+42G>A
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10984
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9628
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7877
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9324
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2571
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2492
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

4-1073390-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1073390
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1073390
    reference: chr 4
allele count: 22
allele frequency: 1.819866322546489e-4
allele num: 120888
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.510+41C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.437+41C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.510+41C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.437+41C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*227-5940C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.363-5940C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*240+41C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*289+41C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.83+41C>T
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2571
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7875
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10984
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 9.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5672
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10034
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4470
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2384
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

4-1073395-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1073395
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1073395
    reference: chr 4
allele count: 2
allele frequency: 1.654588173003739e-5
allele num: 120876
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.83+36C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*289+36C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.437+36C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.510+36C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*227-5945C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.437+36C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.363-5945C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*240+36C>A
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.510+36C>A
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2573
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9651
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9318
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2909
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ

4-1073402-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1073402
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1073402
    reference: chr 4
allele count: 1
allele frequency: 8.273351534706709e-6
allele num: 120870
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.83+29C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.437+29C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.510+29C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.363-5952C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*289+29C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*240+29C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.510+29C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*227-5952C>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.437+29C>T
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9669
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10979
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9313
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4464
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5806
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/4-1073408-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1073408
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 1073408
    reference: chr 4
allele count: 1
allele frequency: 8.273351534706709e-6
allele num: 120870
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000514757
  gene symbol: RNF212
  hgvsc: ENST00000514757.1:n.437+23G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000426115
  ensembl transcript: ENST00000511620
  gene symbol: RNF212
  hgvsc: ENST00000511620.1:c.363-5958G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423030
  ensembl transcript: ENST00000508428
  gene symbol: RNF212
  hgvsc: ENST00000508428.1:c.*240+23G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000503206
  gene symbol: RNF212
  hgvsc: ENST00000503206.1:n.83+23G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl transcript: ENST00000505693
  gene symbol: RNF212
  hgvsc: ENST00000505693.1:n.437+23G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000423560
  ensembl transcript: ENST00000510715
  gene symbol: RNF212
  hgvsc: ENST00000510715.1:c.*227-5958G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000425843
  ensembl transcript: ENST00000506730
  gene symbol: RNF212
  hgvsc: ENST00000506730.1:c.*289+23G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000372428
  ensembl transcript: ENST00000382968
  gene symbol: RNF212
  hgvsc: ENST00000382968.5:c.510+23G>T
  variant of: http://identifiers.org/hgnc/27729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000178222
  ensembl protein: ENSP00000389709
  ensembl transcript: ENST00000433731
  gene symbol: RNF212
  hgvsc: ENST00000433731.2:c.510+23G>T
  variant of: http://identifiers.org/hgnc/27729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9314
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10983
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2483
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5673
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2384
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25750
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2909
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: C

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

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 50954
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5093
bin: 6.75e1
variant carriers: 0

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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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African
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South Asian
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East Asian
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Other
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MQRankSum
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QD
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MQ
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InbreedingCoeff
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BaseQRankSum
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FS
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DP
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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Latino
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African
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European (Non-Finnish)
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Other
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ReadPosRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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VQSLOD
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FS
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ClippingRankSum
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DP
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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European (Finnish)
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South Asian
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Latino
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QD
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MQRankSum
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DP
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FS
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Finnish)
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East Asian
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European (Non-Finnish)
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South Asian
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Other
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FS
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BaseQRankSum
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ReadPosRankSum
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DP
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MQ
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VQSLOD
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InbreedingCoeff
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QD
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MQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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Other
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East Asian
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European (Finnish)
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South Asian
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VQSLOD
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BaseQRankSum
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FS
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MQRankSum
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ReadPosRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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South Asian
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African
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European (Finnish)
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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MQ
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FS
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DP
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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European (Finnish)
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ReadPosRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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QD
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FS
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MQ
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BaseQRankSum
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DP
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East Asian
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MQ
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FS
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InbreedingCoeff
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VQSLOD
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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DP
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QD
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GenotypeQuality
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bin: 9.75e1
variant carriers: 8

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
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: 8
allele frequency: 9.244280101687081e-4
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

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: 10396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66684
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.16e0

VQSLOD
type: SiteQuality
SIO_000300: 3.64e0

MQRankSum
type: SiteQuality
SIO_000300: 2.84e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

DP
type: SiteQuality
SIO_000300: 1.439588e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.4e-1

QD
type: SiteQuality
SIO_000300: 1.376e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 1.178e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.95e-1

GenotypeQuality
all individuals: 1087
bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 50859
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
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: 66680
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.817741153659719e-4
allele num: 16504
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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.41e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.77e-1

FS
type: SiteQuality
SIO_000300: 3.008e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.438914e6

QD
type: SiteQuality
SIO_000300: 1.535e1

MQRankSum
type: SiteQuality
SIO_000300: -2.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.95e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 252
bin: 9.25e1
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: 10390
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
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: 11564
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: 66660
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.843e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-2

DP
type: SiteQuality
SIO_000300: 1.438348e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.626e0

FS
type: SiteQuality
SIO_000300: 4.129e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.384e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 252
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 617
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variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.626492106276473e-5
allele num: 10388
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

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: 11564
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66648
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.805e1

VQSLOD
type: SiteQuality
SIO_000300: -1.366e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.87e-1

FS
type: SiteQuality
SIO_000300: 3.64e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.771e0

MQRankSum
type: SiteQuality
SIO_000300: -1.732e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.09e-1

DP
type: SiteQuality
SIO_000300: 1.438106e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1094
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variant carriers: 0

GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 30
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GenotypeQuality
all individuals: 35
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GenotypeQuality
all individuals: 1085
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 50686
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 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: 8652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66614
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: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.251e0

MQRankSum
type: SiteQuality
SIO_000300: 4.34e-1

MQ
type: SiteQuality
SIO_000300: 5.939e1

QD
type: SiteQuality
SIO_000300: 1.595e1

DP
type: SiteQuality
SIO_000300: 1.437245e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.87e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -8.902e-1

FS
type: SiteQuality
SIO_000300: 9.752000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1092
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1106
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variant carriers: 23

GenotypeQuality
all individuals: 1272
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66600
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

African
type: Population
allele count: 23
allele frequency: 2.216226633262671e-3
allele num: 10378
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.953e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.262e1

VQSLOD
type: SiteQuality
SIO_000300: 2.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.6e-2

MQ
type: SiteQuality
SIO_000300: 5.973e1

FS
type: SiteQuality
SIO_000300: 2.182e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

DP
type: SiteQuality
SIO_000300: 1.437593e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 656
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1040
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GenotypeQuality
all individuals: 1087
bin: 9.75e1
variant carriers: 3

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.264094211976948e-5
allele num: 15964
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.030670384289005e-5
allele num: 65992
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e-1

DP
type: SiteQuality
SIO_000300: 1.404854e6

VQSLOD
type: SiteQuality
SIO_000300: 8.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

QD
type: SiteQuality
SIO_000300: 1.264e1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.1e0

GenotypeQuality
all individuals: 217
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1036
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GenotypeQuality
all individuals: 138
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.031405359524676e-5
allele num: 65976
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
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South Asian
type: Population
allele count: 1
allele frequency: 6.259389083625437e-5
allele num: 15976
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.039e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.97e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.38e-1

DP
type: SiteQuality
SIO_000300: 1.404568e6

QD
type: SiteQuality
SIO_000300: 1.232e1

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.547108039287013e-5
allele num: 65976
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15976
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.404568e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.06e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.38e-1

FS
type: SiteQuality
SIO_000300: 3.039e0

MQRankSum
type: SiteQuality
SIO_000300: 8.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

QD
type: SiteQuality
SIO_000300: 1.232e1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

GenotypeQuality
all individuals: 1087
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10262
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65660
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.406149903907751e-5
allele num: 15610
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

QD
type: SiteQuality
SIO_000300: 1.206e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.677e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.366847e6

GenotypeQuality
all individuals: 418
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15486
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10256
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.525599560627327e-5
allele num: 65548
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.342753e6

QD
type: SiteQuality
SIO_000300: 1.23e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.25e0

VQSLOD
type: SiteQuality
SIO_000300: 7.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.197e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.16e0

MQ
type: SiteQuality
SIO_000300: 5.909e1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65514
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15428
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.765625000000001e-5
allele num: 10240
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.278e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.55e-1

QD
type: SiteQuality
SIO_000300: 1.929e1

FS
type: SiteQuality
SIO_000300: 6.081e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

DP
type: SiteQuality
SIO_000300: 1.332274e6

MQRankSum
type: SiteQuality
SIO_000300: -5.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.6e-2

GenotypeQuality
all individuals: 460
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1919
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65464
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.765625000000001e-5
allele num: 10240
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.99e-1

DP
type: SiteQuality
SIO_000300: 1.326832e6

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-2

QD
type: SiteQuality
SIO_000300: 2.011e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.004e0

MQ
type: SiteQuality
SIO_000300: 5.883e1

VQSLOD
type: SiteQuality
SIO_000300: -2.418e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 57

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 106
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.744316194473592e-5
allele num: 11436
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.784735812133073e-5
allele num: 10220
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

South Asian
type: Population
allele count: 54
allele frequency: 3.528950463991635e-3
allele num: 15302
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529426159305029e-5
allele num: 65384
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.170686022008897e-4
allele num: 8542
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-1

DP
type: SiteQuality
SIO_000300: 1.317117e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.14e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.76e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.803e0

QD
type: SiteQuality
SIO_000300: 1.322e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.57116572479958e-5
allele num: 15218
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65360
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.468e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.47e0

QD
type: SiteQuality
SIO_000300: 1.262e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQ
type: SiteQuality
SIO_000300: 5.843e1

DP
type: SiteQuality
SIO_000300: 1.303333e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.468e0

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.384e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
all individuals: 588
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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.596306068601583e-5
allele num: 15160
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533083951677194e-5
allele num: 65228
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

QD
type: SiteQuality
SIO_000300: 1.467e1

DP
type: SiteQuality
SIO_000300: 1.296696e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.98e-1

FS
type: SiteQuality
SIO_000300: 3.066e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -9.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.179999999999999e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10172
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65098
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.662225183211193e-5
allele num: 15010
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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FS
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SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.7e-1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 8.449999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

MQ
type: SiteQuality
SIO_000300: 5.766e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 10158
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.073518564052127e-5
allele num: 65072
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11402
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DP
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: -4.09e-1

FS
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.165e0

QD
type: SiteQuality
SIO_000300: 1.392e1

MQ
type: SiteQuality
SIO_000300: 5.947e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 19

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11296
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10086
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.179245283018868e-3
allele num: 848
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8398
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 2.789919092346322e-4
allele num: 64518
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.23e-1

QD
type: SiteQuality
SIO_000300: 1.718e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.63e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 3.032e0

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e-1

DP
type: SiteQuality
SIO_000300: 1.255681e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.728e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10286
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508341126429153e-5
allele num: 66298
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16310
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -5.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.21e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.273e0

QD
type: SiteQuality
SIO_000300: 1.295e1

FS
type: SiteQuality
SIO_000300: 3.153e0

VQSLOD
type: SiteQuality
SIO_000300: -8.233e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.55e0

DP
type: SiteQuality
SIO_000300: 1.710782e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.117704637220115e-5
allele num: 16346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66374
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.91e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele num: 894
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

South Asian
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allele count: 2
allele frequency: 1.224589762429586e-4
allele num: 16332
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66352
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European (Finnish)
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African
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VQSLOD
type: SiteQuality
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DP
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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ClippingRankSum
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QD
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FS
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 8.707767328456984e-5
allele num: 11484
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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DP
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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VQSLOD
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MQ
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
type: Population
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African
type: Population
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South Asian
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allele num: 16350
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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MQ
type: SiteQuality
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ReadPosRankSum
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MQRankSum
type: SiteQuality
SIO_000300: -4.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.6e-1

DP
type: SiteQuality
SIO_000300: 1.74903e6

FS
type: SiteQuality
SIO_000300: 3.197e0

VQSLOD
type: SiteQuality
SIO_000300: 5.24e-1

QD
type: SiteQuality
SIO_000300: 1.282e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.659e0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 12

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 36854
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6978
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

South Asian
type: Population
allele count: 13
allele frequency: 7.942326490713588e-4
allele num: 16368
num of homozygotes: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66448
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.33e-1

FS
type: SiteQuality
SIO_000300: 2.958e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.74e-2

QD
type: SiteQuality
SIO_000300: 1.755e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.71e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.758254e6

VQSLOD
type: SiteQuality
SIO_000300: 2.75e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.72e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.009419482981733e-5
allele num: 66458
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.73973556019485e-4
allele num: 11496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157943492357573e-4
allele num: 8636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16378
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.248e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.612e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 1.364e1

MQRankSum
type: SiteQuality
SIO_000300: 7.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.769912e6

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1620
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variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504755025881786e-5
allele num: 66456
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 4.8828125e-4
allele num: 16384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.427e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.41e0

FS
type: SiteQuality
SIO_000300: 2.158e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.05e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.773209e6

VQSLOD
type: SiteQuality
SIO_000300: 2.54e0

MQRankSum
type: SiteQuality
SIO_000300: -1.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.23e-1

GenotypeQuality
all individuals: 110
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
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: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 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: 0
allele frequency: 0.0e0
allele num: 66622
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.779010633379565e-4
allele num: 8652
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.367e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.63e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

DP
type: SiteQuality
SIO_000300: 1.788759e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.53e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.34e-1

QD
type: SiteQuality
SIO_000300: 1.007e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
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: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.500180007200288e-5
allele num: 66664
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.972e1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 8.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.61e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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: 2
allele frequency: 1.733402669440111e-4
allele num: 11538
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66664
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.972e1

MQRankSum
type: SiteQuality
SIO_000300: -1.06e-1

DP
type: SiteQuality
SIO_000300: 1.792682e6

QD
type: SiteQuality
SIO_000300: 1.01e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499835018148004e-5
allele num: 66674
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.952e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 26
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66684
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: 11540
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: 10388
num of homozygotes: 0

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

East Asian
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allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.793193e6

FS
type: SiteQuality
SIO_000300: 6.909999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

QD
type: SiteQuality
SIO_000300: 1.086e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.655e0

MQRankSum
type: SiteQuality
SIO_000300: 1.78e0

VQSLOD
type: SiteQuality
SIO_000300: -1.644e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499610101373643e-5
allele num: 66684
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.77e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.655e0

ReadPosRankSum
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SIO_000300: -1.732e0

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.76e-1

DP
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SIO_000300: 1.793225e6

VQSLOD
type: SiteQuality
SIO_000300: -8.467e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
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: 11542
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e-1

QD
type: SiteQuality
SIO_000300: 1.254e1

MQ
type: SiteQuality
SIO_000300: 5.932e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

DP
type: SiteQuality
SIO_000300: 1.793505e6

FS
type: SiteQuality
SIO_000300: 1.248e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.145e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.667013347200555e-5
allele num: 11538
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: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.793918e6

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

MQ
type: SiteQuality
SIO_000300: 5.867e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.004e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

VQSLOD
type: SiteQuality
SIO_000300: -1.241e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.125e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.36e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
type: Population
allele count: 1
allele frequency: 8.679048776254123e-5
allele num: 11522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 28
allele frequency: 4.200672107537206e-4
allele num: 66656
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.635767970707265e-5
allele num: 10378
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.641660597232338e-4
allele num: 16476
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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VQSLOD
type: SiteQuality
SIO_000300: 2.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.07e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

FS
type: SiteQuality
SIO_000300: 5.35e-1

MQRankSum
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SIO_000300: -7.5e-2

MQ
type: SiteQuality
SIO_000300: 5.971e1

BaseQRankSum
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SIO_000300: 6.01e-1

QD
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SIO_000300: 1.209e1

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.000750187546887e-5
allele num: 66650
num of homozygotes: 0

Other
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num of homozygotes: 0

FS
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QD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500600240096038e-5
allele num: 66640
num of homozygotes: 0

East Asian
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Latino
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 1.457725947521866e-3
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Other
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allele num: 906
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QD
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BaseQRankSum
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InbreedingCoeff
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FS
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VQSLOD
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MQ
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 3
allele frequency: 3.470615455807496e-4
allele num: 8644
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.501231009427731e-5
allele num: 66612
num of homozygotes: 0

Latino
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Other
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South Asian
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European (Finnish)
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VQSLOD
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MQ
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DP
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ReadPosRankSum
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FS
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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allele frequency: 6.077549532028686e-5
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 9.658103148541626e-5
allele num: 10354
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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ReadPosRankSum
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MQ
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FS
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MQRankSum
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VQSLOD
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InbreedingCoeff
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DP
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QD
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16376
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11466
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.505797319680771e-5
allele num: 66410
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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FS
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QD
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DP
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MQRankSum
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VQSLOD
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MQ
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
allele num: 10302
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8614
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

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

South Asian
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allele frequency: 1.223690651003426e-4
allele num: 16344
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ReadPosRankSum
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SIO_000300: 6.15e-1

MQ
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InbreedingCoeff
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DP
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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FS
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.513179796023364e-5
allele num: 66086
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11416
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10270
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.088e1

InbreedingCoeff
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SIO_000300: 2.6e-3

ReadPosRankSum
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MQRankSum
type: SiteQuality
SIO_000300: 7.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.6e-2

DP
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BaseQRankSum
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SIO_000300: -2.597e0

VQSLOD
type: SiteQuality
SIO_000300: 7.86e-1

FS
type: SiteQuality
SIO_000300: 3.77e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65972
num of homozygotes: 0

Latino
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allele num: 11408
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele num: 8570
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African
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allele frequency: 9.75800156128025e-5
allele num: 10248
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.731407e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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MQ
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BaseQRankSum
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MQRankSum
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

VQSLOD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

South Asian
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East Asian
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Other
type: Population
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European (Non-Finnish)
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European (Finnish)
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African
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allele num: 10248
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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MQRankSum
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BaseQRankSum
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DP
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FS
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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num of homozygotes: 0

Latino
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 65748
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South Asian
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European (Finnish)
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DP
type: SiteQuality
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MQ
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QD
type: SiteQuality
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MQRankSum
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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African
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Other
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South Asian
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European (Non-Finnish)
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Latino
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ReadPosRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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MQ
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MQRankSum
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VQSLOD
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ClippingRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.529660109523664e-5
allele num: 65374
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11276
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
allele num: 16084
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Other
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allele frequency: 0.0e0
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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FS
type: SiteQuality
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DP
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QD
type: SiteQuality
SIO_000300: 1.877e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.664e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11268
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 10126
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8450
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.530690341343946e-5
allele num: 65330
num of homozygotes: 0

South Asian
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allele frequency: 6.219679064560268e-5
allele num: 16078
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Other
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ReadPosRankSum
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BaseQRankSum
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DP
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QD
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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FS
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SIO_000300: 4.721e0

MQ
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SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele frequency: 8.944543828264758e-5
allele num: 11180
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15944
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6446
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64782
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10046
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
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East Asian
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allele frequency: 0.0e0
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InbreedingCoeff
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QD
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ReadPosRankSum
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SIO_000300: 3.91e-1

BaseQRankSum
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ClippingRankSum
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DP
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FS
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VQSLOD
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MQ
type: SiteQuality
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MQRankSum
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SIO_000300: 4.4e-2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 70

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11180
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.128668171557562e-3
allele num: 886
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6446
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.195028680688336e-4
allele num: 8368
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 69
allele frequency: 4.327646763672855e-3
allele num: 15944
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.543638665061283e-5
allele num: 64782
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.49e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.91e-1

QD
type: SiteQuality
SIO_000300: 1.314e1

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.56e0

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 30

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16022
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 26
allele frequency: 4.001107999138223e-4
allele num: 64982
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6476
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8378
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10070
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Latino
type: Population
allele count: 3
allele frequency: 2.680965147453083e-4
allele num: 11190
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.75e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.08e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.519374e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15828
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.095050372317127e-4
allele num: 63924
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11000
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European (Finnish)
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allele count: 4
allele frequency: 6.273525721455458e-4
allele num: 6376
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East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 872
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.82e-1

FS
type: SiteQuality
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BaseQRankSum
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DP
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QD
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ClippingRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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MQRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6370
num of homozygotes: 0

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

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

African
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allele count: 0
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Other
type: Population
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.564651395669045e-5
allele num: 63912
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
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FS
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MQ
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 2
allele frequency: 1.944012441679627e-4
allele num: 10288
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66434
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.13e-1

ReadPosRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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FS
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QD
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DP
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BaseQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 41
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variant carriers: 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: 66432
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10290
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.318034306907742e-4
allele num: 8628
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
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: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.680681e6

VQSLOD
type: SiteQuality
SIO_000300: 9.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.009e0

MQRankSum
type: SiteQuality
SIO_000300: 1.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

FS
type: SiteQuality
SIO_000300: 5.135e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.0e-1

QD
type: SiteQuality
SIO_000300: 1.192e1

GenotypeQuality
all individuals: 52
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2912
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4472
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2385
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10290
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.213886865744113e-4
allele num: 16476
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: 8628
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66428
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: 11546
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.588e0

FS
type: SiteQuality
SIO_000300: 1.8784e1

MQ
type: SiteQuality
SIO_000300: 5.984e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.84e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.47e-1

QD
type: SiteQuality
SIO_000300: 1.324e1

DP
type: SiteQuality
SIO_000300: 2.680665e6

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 22

GenotypeQuality
all individuals: 84
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10290
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: 66426
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: 22
allele frequency: 2.549837737598517e-3
allele num: 8628
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.17e-1

DP
type: SiteQuality
SIO_000300: 2.680908e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.812e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.6e-2

MQRankSum
type: SiteQuality
SIO_000300: -9.1e-2

QD
type: SiteQuality
SIO_000300: 1.23e1

VQSLOD
type: SiteQuality
SIO_000300: 3.3e0

GenotypeQuality
all individuals: 2384
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25755
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3997
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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: 2
allele frequency: 3.011231894968231e-5
allele num: 66418
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.830000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.167e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

QD
type: SiteQuality
SIO_000300: 1.146e1

DP
type: SiteQuality
SIO_000300: 2.679761e6

MQ
type: SiteQuality
SIO_000300: 5.95e1

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

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2907
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.662508662508663e-5
allele num: 11544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
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: 66424
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.895e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.37e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

FS
type: SiteQuality
SIO_000300: 2.686e0

QD
type: SiteQuality
SIO_000300: 1.218e1

DP
type: SiteQuality
SIO_000300: 2.679779e6

GenotypeQuality
all individuals: 5812
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0