4-945462-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 945462
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 945462
    reference: chr 4
allele count: 4
allele frequency: 3.296087544085171e-5
allele num: 121356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*326-8C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.343-8C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.454-8C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.916-8C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.97-8C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.97-8C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.-14C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.96+416C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.343-8C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.381C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.304-8C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.904-8C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000502513
  gene symbol: TMEM175
  hgvsc: ENST00000502513.1:n.121-8C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.97-8C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*357C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427626
  ensembl transcript: ENST00000513682
  gene symbol: TMEM175
  hgvsc: ENST00000513682.1:c.*214-8C>G
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5724
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2729
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.343-8C>G
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

4-945462-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 945462
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 945462
    reference: chr 4
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427626
  ensembl transcript: ENST00000513682
  gene symbol: TMEM175
  hgvsc: ENST00000513682.1:c.*214-8C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.343-8C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*326-8C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.904-8C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.304-8C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.-14C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.96+416C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.454-8C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.343-8C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.97-8C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.97-8C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.916-8C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.97-8C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.381C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000502513
  gene symbol: TMEM175
  hgvsc: ENST00000502513.1:n.121-8C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*357C>T
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5724
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.343-8C>T
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP

4-945464-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 945464
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 945464
    reference: chr 4
allele count: 2
allele frequency: 1.647962294622699e-5
allele num: 121362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.916-6C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.96+418C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.383C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.343-6C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*359C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.97-6C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*326-6C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.304-6C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.97-6C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427626
  ensembl transcript: ENST00000513682
  gene symbol: TMEM175
  hgvsc: ENST00000513682.1:c.*214-6C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000502513
  gene symbol: TMEM175
  hgvsc: ENST00000502513.1:n.121-6C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.343-6C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.904-6C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.454-6C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.97-6C>T
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6008
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5724
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.343-6C>T
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

4-945474-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 945474
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 945474
    reference: chr 4
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.908G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.101G>C
  hgvsp: ENSP00000423669.1:p.Cys34Ser
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.101G>C
  hgvsp: ENSP00000424208.1:p.Cys34Ser
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.-2G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*369G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000502513
  gene symbol: TMEM175
  hgvsc: ENST00000502513.1:n.125G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.920G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.393G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.347G>C
  hgvsp: ENSP00000264771.4:p.Cys116Ser
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427626
  ensembl transcript: ENST00000513682
  gene symbol: TMEM175
  hgvsc: ENST00000513682.1:c.*218G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.347G>C
  hgvsp: ENSP00000425763.1:p.Cys116Ser
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*330G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.101G>C
  hgvsp: ENSP00000425867.1:p.Cys34Ser
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.308G>C
  hgvsp: ENSP00000425181.1:p.Cys103Ser
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.458G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.96+428G>C
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6008
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5571
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys116Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/4-945484-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 945484
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 945484
    reference: chr 4
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.930C>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.357C>A
  hgvsp: ENST00000514546.1:c.357C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.111C>A
  hgvsp: ENST00000510493.1:c.111C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*379C>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.9C>A
  hgvsp: ENST00000515740.1:c.9C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.468C>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427626
  ensembl transcript: ENST00000513682
  gene symbol: TMEM175
  hgvsc: ENST00000513682.1:c.*228C>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.111C>A
  hgvsp: ENST00000508204.1:c.111C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.318C>A
  hgvsp: ENST00000514453.1:c.318C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.918C>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.357C>A
  hgvsp: ENST00000264771.4:c.357C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000502513
  gene symbol: TMEM175
  hgvsc: ENST00000502513.1:n.135C>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.111C>A
  hgvsp: ENST00000515492.1:c.111C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*340C>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.403C>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.96+438C>A
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr119Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD

4-945498-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 945498
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 945498
    reference: chr 4
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.371C>T
  hgvsp: ENSP00000264771.4:p.Pro124Leu
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.96+452C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.482C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*354C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.125C>T
  hgvsp: ENSP00000424208.1:p.Pro42Leu
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.417C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*393C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.332C>T
  hgvsp: ENSP00000425181.1:p.Pro111Leu
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.371C>T
  hgvsp: ENSP00000425763.1:p.Pro124Leu
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000502513
  gene symbol: TMEM175
  hgvsc: ENST00000502513.1:n.149C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.23C>T
  hgvsp: ENSP00000427039.1:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.125C>T
  hgvsp: ENSP00000425867.1:p.Pro42Leu
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.944C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.125C>T
  hgvsp: ENSP00000423669.1:p.Pro42Leu
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.932C>T
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro124Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

4-945500-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 945500
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 945500
    reference: chr 4
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.127T>C
  hgvsp: ENSP00000424208.1:p.Tyr43His
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.484T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.373T>C
  hgvsp: ENSP00000425763.1:p.Tyr125His
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.946T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*356T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.127T>C
  hgvsp: ENSP00000423669.1:p.Tyr43His
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.96+454T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000502513
  gene symbol: TMEM175
  hgvsc: ENST00000502513.1:n.151T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.419T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.25T>C
  hgvsp: ENSP00000427039.1:p.Tyr9His
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.334T>C
  hgvsp: ENSP00000425181.1:p.Tyr112His
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.373T>C
  hgvsp: ENSP00000264771.4:p.Tyr125His
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*395T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.934T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.127T>C
  hgvsp: ENSP00000425867.1:p.Tyr43His
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5717
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr125His
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

4-945502-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 945502
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 945502
    reference: chr 4
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.936C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.27C>T
  hgvsp: ENST00000515740.1:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.421C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.948C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.375C>T
  hgvsp: ENST00000514546.1:c.375C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*358C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.486C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*397C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.129C>T
  hgvsp: ENST00000515492.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000502513
  gene symbol: TMEM175
  hgvsc: ENST00000502513.1:n.153C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.336C>T
  hgvsp: ENST00000514453.1:c.336C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.375C>T
  hgvsp: ENST00000264771.4:c.375C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.129C>T
  hgvsp: ENST00000510493.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.96+456C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.129C>T
  hgvsp: ENST00000508204.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6008
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2729
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr125Tyr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

4-945504-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 945504
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 945504
    reference: chr 4
allele count: 5
allele frequency: 4.120313143798929e-5
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.377C>T
  hgvsp: ENSP00000264771.4:p.Thr126Met
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000502513
  gene symbol: TMEM175
  hgvsc: ENST00000502513.1:n.155C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.131C>T
  hgvsp: ENSP00000424208.1:p.Thr44Met
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.488C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*399C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.950C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.338C>T
  hgvsp: ENSP00000425181.1:p.Thr113Met
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.131C>T
  hgvsp: ENSP00000423669.1:p.Thr44Met
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.377C>T
  hgvsp: ENSP00000425763.1:p.Thr126Met
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*360C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.29C>T
  hgvsp: ENSP00000427039.1:p.Thr10Met
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.938C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.131C>T
  hgvsp: ENSP00000425867.1:p.Thr44Met
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.423C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.96+458C>T
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6008
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5716
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4670
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr126Met
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ

4-945505-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 945505
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 945505
    reference: chr 4
allele count: 2
allele frequency: 1.648206751054852e-5
allele num: 121344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.132G>A
  hgvsp: ENST00000508204.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*361G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.378G>A
  hgvsp: ENST00000514546.1:c.378G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.424G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000502513
  gene symbol: TMEM175
  hgvsc: ENST00000502513.1:n.156G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.30G>A
  hgvsp: ENST00000515740.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.96+459G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.132G>A
  hgvsp: ENST00000510493.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.339G>A
  hgvsp: ENST00000514453.1:c.339G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*400G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.951G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.489G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.132G>A
  hgvsp: ENST00000515492.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.378G>A
  hgvsp: ENST00000264771.4:c.378G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.939G>A
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.378G>A
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

4-945508-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 945508
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 945508
    reference: chr 4
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*361+3G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.939+3G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.339+3G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.378+3G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.424+3G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.378+3G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.951+3G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.132+3G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*400+3G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.30+3G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.132+3G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.96+462G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.132+3G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.489+3G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000502513
  gene symbol: TMEM175
  hgvsc: ENST00000502513.1:n.159G>A
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6008
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2735
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.378+3G>A
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

4-945510-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 945510
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 945510
    reference: chr 4
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.132+5G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.951+5G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.339+5G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*400+5G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.489+5G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.939+5G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000502513
  gene symbol: TMEM175
  hgvsc: ENST00000502513.1:n.161G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.30+5G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.424+5G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.378+5G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.378+5G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.96+464G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.132+5G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.132+5G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*361+5G>A
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5567
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5716
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.378+5G>A
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-945510-GCAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 945510
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 945507
    reference: chr 4
allele count: 28
allele frequency: 2.307413389590269e-4
allele num: 121348
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.132+8_132+10delACA
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.132+8_132+10delACA
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*361+8_*361+10delACA
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000502513
  gene symbol: TMEM175
  hgvsc: ENST00000502513.1:n.164_166delACA
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.96+467_96+469delACA
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.30+8_30+10delACA
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.339+8_339+10delACA
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.951+8_951+10delACA
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.489+8_489+10delACA
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*400+8_*400+10delACA
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.378+8_378+10delACA
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.939+8_939+10delACA
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.424+8_424+10delACA
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.132+8_132+10delACA
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.378+8_378+10delACA
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5567
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2730
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.378+8_378+10delACA
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: GCAA
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

4-945514-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 945514
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 945514
    reference: chr 4
allele count: 1
allele frequency: 8.244838730954422e-6
allele num: 121288
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.939+9C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.132+9C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.339+9C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*361+9C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.132+9C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.951+9C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.489+9C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*400+9C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.378+9C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000502513
  gene symbol: TMEM175
  hgvsc: ENST00000502513.1:n.165C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.96+468C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.132+9C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.378+9C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.30+9C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.424+9C>T
  variant of: http://identifiers.org/hgnc/28709
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5711
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6008
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

4-945516-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 945516
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 945516
    reference: chr 4
allele count: 88
allele frequency: 7.252229236373226e-4
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000502513
  gene symbol: TMEM175
  hgvsc: ENST00000502513.1:n.167C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.951+11C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.378+11C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*361+11C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.96+470C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.132+11C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.424+11C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.339+11C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.132+11C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.132+11C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.489+11C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.939+11C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*400+11C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.30+11C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.378+11C>T
  variant of: http://identifiers.org/hgnc/28709
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4233
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3528
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

4-945519-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 945519
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 945519
    reference: chr 4
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.30+14G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.378+14G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.489+14G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*361+14G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000502513
  gene symbol: TMEM175
  hgvsc: ENST00000502513.1:n.170G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.339+14G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.939+14G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*400+14G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.951+14G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.424+14G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.378+14G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.132+14G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.132+14G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.132+14G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.96+473G>C
  variant of: http://identifiers.org/hgnc/28709
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5667
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5574
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2266
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5732
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD

4-945532-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 945532
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 945532
    reference: chr 4
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.132+27C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.378+27C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.951+27C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000502513
  gene symbol: TMEM175
  hgvsc: ENST00000502513.1:n.183C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.489+27C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.30+27C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.132+27C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.96+486C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.339+27C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.424+27C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*361+27C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.378+27C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.939+27C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.132+27C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*400+27C>T
  variant of: http://identifiers.org/hgnc/28709
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2735
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5732
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2266
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

4-945544-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 945544
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 945544
    reference: chr 4
allele count: 3
allele frequency: 2.473533194815474e-5
allele num: 121284
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000502513
  gene symbol: TMEM175
  hgvsc: ENST00000502513.1:n.195T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.378+39T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.424+39T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.378+39T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*361+39T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.489+39T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.132+39T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.30+39T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.132+39T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.951+39T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.132+39T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.339+39T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.939+39T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*400+39T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.96+498T>C
  variant of: http://identifiers.org/hgnc/28709
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5124
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

4-946111-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946111
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946111
    reference: chr 4
allele count: 1
allele frequency: 8.357709987463435e-6
allele num: 119650
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.379-44A>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.379-44A>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*362-44A>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.490-44A>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.425-44A>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.133-44A>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.31-44A>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.97-44A>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.340-44A>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.952-44A>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*401-44A>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.133-44A>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.940-44A>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.133-44A>G
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7736
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5458
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6354
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5011
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7479
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

4-946114-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946114
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946114
    reference: chr 4
allele count: 1
allele frequency: 8.353660574063554e-6
allele num: 119708
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.340-41C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.425-41C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.940-41C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.379-41C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*362-41C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.133-41C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.133-41C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*401-41C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.133-41C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.379-41C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.31-41C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.490-41C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.952-41C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.97-41C>G
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7491
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7305
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5513
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7777
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

4-946121-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946121
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946121
    reference: chr 4
allele count: 58
allele frequency: 4.835348061692372e-4
allele num: 119950
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*362-34T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.379-34T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.31-34T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*401-34T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.133-34T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.490-34T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.340-34T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.133-34T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.97-34T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.133-34T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.379-34T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.940-34T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.952-34T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.425-34T>G
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7467
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7844
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5707
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6433
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 5461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 6.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

4-946122-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946122
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946123
    reference: chr 4
allele count: 31
allele frequency: 2.592363399173789e-4
allele num: 119582
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.379-26dupG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*362-26dupG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.97-26dupG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.31-26dupG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.133-26dupG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.133-26dupG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.340-26dupG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.952-26dupG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.490-26dupG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.940-26dupG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.425-26dupG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.379-26dupG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.133-26dupG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*401-26dupG
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5745
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7513
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7886
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6454
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5386
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 5044
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS

4-946122-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946122
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946121
    reference: chr 4
allele count: 1
allele frequency: 8.362462577979963e-6
allele num: 119582
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.490-26delG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.133-26delG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.340-26delG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*401-26delG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.133-26delG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.133-26delG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*362-26delG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.940-26delG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.97-26delG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.31-26delG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.952-26delG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.379-26delG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.425-26delG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.379-26delG
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 7513
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7551
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7886
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6454
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5745
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: TG
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP

4-946123-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946123
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946123
    reference: chr 4
allele count: 1
allele frequency: 8.34153584357952e-6
allele num: 119882
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.379-32G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*401-32G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.133-32G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.952-32G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.133-32G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.133-32G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.97-32G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.490-32G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.940-32G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*362-32G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.340-32G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.31-32G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.379-32G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.425-32G>C
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6470
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7568
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5779
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3685
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7514
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD

4-946124-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946124
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946124
    reference: chr 4
allele count: 1
allele frequency: 8.315731701232391e-6
allele num: 120254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.379-31G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.940-31G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.490-31G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*401-31G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.97-31G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.31-31G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.133-31G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.340-31G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.425-31G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.133-31G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*362-31G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.379-31G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.952-31G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.133-31G>A
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5786
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3689
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7546
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ

4-946124-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946124
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946124
    reference: chr 4
allele count: 1
allele frequency: 8.315731701232391e-6
allele num: 120254
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*401-31G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.940-31G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.490-31G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.133-31G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.379-31G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.425-31G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.31-31G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.97-31G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.340-31G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.379-31G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.133-31G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*362-31G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.952-31G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.133-31G>C
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7546
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5786
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ

4-946130-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946130
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946130
    reference: chr 4
allele count: 20
allele frequency: 1.659558225600345e-4
allele num: 120514
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.952-25T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.31-25T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.133-25T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.97-25T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.379-25T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.379-25T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.340-25T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.940-25T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.490-25T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.425-25T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.133-25T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*401-25T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*362-25T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.133-25T>G
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5604
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7647
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5826
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6503
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7595
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

4-946133-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946133
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946133
    reference: chr 4
allele count: 3
allele frequency: 2.486490070616318e-5
allele num: 120652
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.379-22G>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.952-22G>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.133-22G>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.133-22G>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.490-22G>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*362-22G>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.379-22G>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.340-22G>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*401-22G>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.425-22G>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.97-22G>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.940-22G>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.31-22G>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.133-22G>T
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7970
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7676
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5860
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6506
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum

4-946140-TTTTTG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946140
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946135
    reference: chr 4
allele count: 1
allele frequency: 8.275816409288777e-6
allele num: 120834
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.952-10_952-6delGTTTT
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.133-10_133-6delGTTTT
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*401-10_*401-6delGTTTT
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.31-10_31-6delGTTTT
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.379-10_379-6delGTTTT
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.379-10_379-6delGTTTT
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.340-10_340-6delGTTTT
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.490-10_490-6delGTTTT
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.97-10_97-6delGTTTT
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.940-10_940-6delGTTTT
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.133-10_133-6delGTTTT
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.133-10_133-6delGTTTT
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*362-10_*362-6delGTTTT
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.425-10_425-6delGTTTT
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5923
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5907
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7976
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5062
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: TTTTTG
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

4-946143-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946143
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946143
    reference: chr 4
allele count: 117
allele frequency: 9.678540112171798e-4
allele num: 120886
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.133-12T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.97-12T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.379-12T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*362-12T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.379-12T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.31-12T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.133-12T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*401-12T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.425-12T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.952-12T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.490-12T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.133-12T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.940-12T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.340-12T>C
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5944
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6493
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5919
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 9.75e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 7967
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5051
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 1
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

4-946144-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946144
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946144
    reference: chr 4
allele count: 1
allele frequency: 8.271161767381846e-6
allele num: 120902
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.133-11T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.490-11T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.133-11T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.340-11T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.379-11T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*401-11T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.940-11T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*362-11T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.379-11T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.952-11T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.31-11T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.425-11T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.97-11T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.133-11T>C
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5052
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7967
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7695
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ

4-946145-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946145
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946145
    reference: chr 4
allele count: 1
allele frequency: 8.271024945411235e-6
allele num: 120904
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.490-10G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.133-10G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.340-10G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.133-10G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*362-10G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.940-10G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.133-10G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.952-10G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.31-10G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.379-10G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*401-10G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.97-10G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.379-10G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.425-10G>A
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5924
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7965
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6491
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ

4-946152-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946152
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946152
    reference: chr 4
allele count: 2
allele frequency: 1.652974527662529e-5
allele num: 120994
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.952-3C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.340-3C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.133-3C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.133-3C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.425-3C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.379-3C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*362-3C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*401-3C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.379-3C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.490-3C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.97-3C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.31-3C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.940-3C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.133-3C>T
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5941
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7706
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7970
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7609
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.379-3C>T
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

4-946159-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946159
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946159
    reference: chr 4
allele count: 1
allele frequency: 8.260230295220631e-6
allele num: 121062
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*405C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.137C>T
  hgvsp: ENSP00000425867.1:p.Ser46Leu
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.383C>T
  hgvsp: ENSP00000264771.4:p.Ser128Leu
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.344C>T
  hgvsp: ENSP00000425181.1:p.Ser115Leu
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*366C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.956C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.494C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.101C>T
  hgvsp: ENSP00000421750.1:p.Ser34Leu
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.383C>T
  hgvsp: ENSP00000425763.1:p.Ser128Leu
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.944C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.137C>T
  hgvsp: ENSP00000424208.1:p.Ser46Leu
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.137C>T
  hgvsp: ENSP00000423669.1:p.Ser46Leu
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.429C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.35C>T
  hgvsp: ENSP00000427039.1:p.Ser12Leu
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3694
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5953
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7611
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser128Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

4-946160-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946160
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946160
    reference: chr 4
allele count: 5
allele frequency: 4.129569368506252e-5
allele num: 121078
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.102G>A
  hgvsp: ENST00000509508.1:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*367G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.138G>A
  hgvsp: ENST00000515492.1:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.138G>A
  hgvsp: ENST00000510493.1:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.36G>A
  hgvsp: ENST00000515740.1:c.36G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.945G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.430G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.495G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.345G>A
  hgvsp: ENST00000514453.1:c.345G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*406G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425763
  ensembl transcript: ENST00000514546
  gene symbol: TMEM175
  hgvsc: ENST00000514546.1:c.384G>A
  hgvsp: ENST00000514546.1:c.384G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.138G>A
  hgvsp: ENST00000508204.1:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.957G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.384G>A
  hgvsp: ENST00000264771.4:c.384G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7610
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6056
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser128Ser
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

4-946179-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946179
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946179
    reference: chr 4
allele count: 1
allele frequency: 8.252595441266279e-6
allele num: 121174
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.964G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.157G>A
  hgvsp: ENSP00000425867.1:p.Asp53Asn
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.55G>A
  hgvsp: ENSP00000427039.1:p.Asp19Asn
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.364G>A
  hgvsp: ENSP00000425181.1:p.Asp122Asn
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.157G>A
  hgvsp: ENSP00000424208.1:p.Asp53Asn
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.514G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.403G>A
  hgvsp: ENSP00000264771.4:p.Asp135Asn
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.121G>A
  hgvsp: ENSP00000421750.1:p.Asp41Asn
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*386G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*425G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.157G>A
  hgvsp: ENSP00000423669.1:p.Asp53Asn
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.976G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.449G>A
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7613
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7971
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6059
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7737
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5978
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp135Asn
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-946181-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946181
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946181
    reference: chr 4
allele count: 1
allele frequency: 8.252323028932645e-6
allele num: 121178
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*388T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*427T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.57T>C
  hgvsp: ENST00000515740.1:c.57T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.451T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.405T>C
  hgvsp: ENST00000264771.4:c.405T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.123T>C
  hgvsp: ENST00000509508.1:c.123T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.159T>C
  hgvsp: ENST00000515492.1:c.159T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.159T>C
  hgvsp: ENST00000510493.1:c.159T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.366T>C
  hgvsp: ENST00000514453.1:c.366T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.966T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.978T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.516T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.159T>C
  hgvsp: ENST00000508204.1:c.159T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7612
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7972
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6048
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp135Asp
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

4-946187-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946187
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946187
    reference: chr 4
allele count: 1
allele frequency: 8.251642076773278e-6
allele num: 121188
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.165T>C
  hgvsp: ENST00000515492.1:c.165T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.457T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.63T>C
  hgvsp: ENST00000515740.1:c.63T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.129T>C
  hgvsp: ENST00000509508.1:c.129T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.411T>C
  hgvsp: ENST00000264771.4:c.411T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.165T>C
  hgvsp: ENST00000510493.1:c.165T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.984T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.165T>C
  hgvsp: ENST00000508204.1:c.165T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*433T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.372T>C
  hgvsp: ENST00000514453.1:c.372T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*394T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.522T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.972T>C
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5993
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6494
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7612
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7971
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6021
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro137Pro
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

4-946193-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946193
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946193
    reference: chr 4
allele count: 1
allele frequency: 8.250961236984109e-6
allele num: 121198
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.417C>T
  hgvsp: ENST00000264771.4:c.417C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.990C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.378C>T
  hgvsp: ENST00000514453.1:c.378C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.135C>T
  hgvsp: ENST00000509508.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.978C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.171C>T
  hgvsp: ENST00000510493.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*439C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.171C>T
  hgvsp: ENST00000515492.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.463C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.69C>T
  hgvsp: ENST00000515740.1:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*400C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.528C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.171C>T
  hgvsp: ENST00000508204.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6494
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5995
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly139Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

4-946194-ATCT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946194
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946191
    reference: chr 4
allele count: 1
allele frequency: 8.250961236984109e-6
allele num: 121198
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.423_425delCTT
  hgvsp: ENSP00000264771.4:p.Phe141del
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*445_*447delCTT
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*406_*408delCTT
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.984_986delCTT
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.177_179delCTT
  hgvsp: ENSP00000423669.1:p.Phe59del
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.75_77delCTT
  hgvsp: ENSP00000427039.1:p.Phe25del
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.177_179delCTT
  hgvsp: ENSP00000425867.1:p.Phe59del
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.534_536delCTT
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.177_179delCTT
  hgvsp: ENSP00000424208.1:p.Phe59del
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.384_386delCTT
  hgvsp: ENSP00000425181.1:p.Phe128del
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.996_998delCTT
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.141_143delCTT
  hgvsp: ENSP00000421750.1:p.Phe47del
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.469_471delCTT
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7612
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe141del
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: ATCT
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

4-946200-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946200
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946200
    reference: chr 4
allele count: 4
allele frequency: 3.300275573010346e-5
allele num: 121202
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.76T>A
  hgvsp: ENSP00000427039.1:p.Leu26Met
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.385T>A
  hgvsp: ENSP00000425181.1:p.Leu129Met
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*407T>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.470T>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.997T>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.178T>A
  hgvsp: ENSP00000425867.1:p.Leu60Met
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.535T>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.178T>A
  hgvsp: ENSP00000424208.1:p.Leu60Met
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.142T>A
  hgvsp: ENSP00000421750.1:p.Leu48Met
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.424T>A
  hgvsp: ENSP00000264771.4:p.Leu142Met
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*446T>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.178T>A
  hgvsp: ENSP00000423669.1:p.Leu60Met
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000506669
  gene symbol: TMEM175
  hgvsc: ENST00000506669.1:n.2T>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.985T>A
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7970
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7612
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5981
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu142Met
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

4-946202-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946202
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946202
    reference: chr 4
allele count: 4
allele frequency: 3.300384494793644e-5
allele num: 121198
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.144G>C
  hgvsp: ENSP00000421750.1:p.Leu48Phe
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.180G>C
  hgvsp: ENSP00000424208.1:p.Leu60Phe
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*409G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.180G>C
  hgvsp: ENSP00000423669.1:p.Leu60Phe
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.999G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.426G>C
  hgvsp: ENSP00000264771.4:p.Leu142Phe
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.78G>C
  hgvsp: ENSP00000427039.1:p.Leu26Phe
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.537G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.987G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.472G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.387G>C
  hgvsp: ENSP00000425181.1:p.Leu129Phe
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.180G>C
  hgvsp: ENSP00000425867.1:p.Leu60Phe
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*448G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000506669
  gene symbol: TMEM175
  hgvsc: ENST00000506669.1:n.4G>C
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6002
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5970
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu142Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD

4-946205-C-CTG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946205
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946207
    reference: chr 4
allele count: 1
allele frequency: 8.263233568560049e-6
allele num: 121018
alternate allele: CTG
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.194_195dupTG
  hgvsp: ENSP00000425867.1:p.Ile66Ter
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.486_487dupTG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.1013_1014dupTG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.194_195dupTG
  hgvsp: ENSP00000424208.1:p.Ile66Ter
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.551_552dupTG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*423_*424dupTG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.401_402dupTG
  hgvsp: ENSP00000425181.1:p.Ile135Ter
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.440_441dupTG
  hgvsp: ENSP00000264771.4:p.Ile148Ter
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000506669
  gene symbol: TMEM175
  hgvsc: ENST00000506669.1:n.18_19dupTG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.158_159dupTG
  hgvsp: ENSP00000421750.1:p.Ile54Ter
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.194_195dupTG
  hgvsp: ENSP00000423669.1:p.Ile66Ter
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.92_93dupTG
  hgvsp: ENSP00000427039.1:p.Ile32Ter
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.1001_1002dupTG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*462_*463dupTG
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7965
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3688
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5879
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile148Ter
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

4-946205-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946205
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946205
    reference: chr 4
allele count: 4
allele frequency: 3.305293427424019e-5
allele num: 121018
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.183C>G
  hgvsp: ENSP00000423669.1:p.Phe61Leu
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.390C>G
  hgvsp: ENSP00000425181.1:p.Phe130Leu
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.147C>G
  hgvsp: ENSP00000421750.1:p.Phe49Leu
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.429C>G
  hgvsp: ENSP00000264771.4:p.Phe143Leu
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.81C>G
  hgvsp: ENSP00000427039.1:p.Phe27Leu
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.540C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.183C>G
  hgvsp: ENSP00000424208.1:p.Phe61Leu
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.475C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*451C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.1002C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.990C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.183C>G
  hgvsp: ENSP00000425867.1:p.Phe61Leu
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*412C>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000506669
  gene symbol: TMEM175
  hgvsc: ENST00000506669.1:n.7C>G
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe143Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD

4-946205-CTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946205
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946203
    reference: chr 4
allele count: 12
allele frequency: 9.915880282272059e-5
allele num: 121018
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.194_195delTG
  hgvsp: ENSP00000423669.1:p.Val65AspfsTer104
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.1013_1014delTG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.194_195delTG
  hgvsp: ENSP00000425867.1:p.Val65AspfsTer104
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.486_487delTG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.440_441delTG
  hgvsp: ENSP00000264771.4:p.Val147AspfsTer104
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*423_*424delTG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.194_195delTG
  hgvsp: ENSP00000424208.1:p.Val65AspfsTer104
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000506669
  gene symbol: TMEM175
  hgvsc: ENST00000506669.1:n.18_19delTG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.401_402delTG
  hgvsp: ENSP00000425181.1:p.Val134AspfsTer?
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.92_93delTG
  hgvsp: ENSP00000427039.1:p.Val31AspfsTer104
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.1001_1002delTG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.158_159delTG
  hgvsp: ENSP00000421750.1:p.Val53AspfsTer104
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*462_*463delTG
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.551_552delTG
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5966
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7965
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5879
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7617
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val147AspfsTer104
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: CTG
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

4-946208-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946208
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946208
    reference: chr 4
allele count: 1
allele frequency: 8.262687356435807e-6
allele num: 121026
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.543T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.186T>C
  hgvsp: ENST00000510493.1:c.186T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.432T>C
  hgvsp: ENST00000264771.4:c.432T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.186T>C
  hgvsp: ENST00000508204.1:c.186T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.84T>C
  hgvsp: ENST00000515740.1:c.84T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.393T>C
  hgvsp: ENST00000514453.1:c.393T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*415T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.993T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*454T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.186T>C
  hgvsp: ENST00000515492.1:c.186T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.150T>C
  hgvsp: ENST00000509508.1:c.150T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000506669
  gene symbol: TMEM175
  hgvsc: ENST00000506669.1:n.10T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.478T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.1005T>C
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7735
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6495
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5849
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys144Cys
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff

4-946213-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946213
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946213
    reference: chr 4
allele count: 1
allele frequency: 8.255865792645674e-6
allele num: 121126
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.548G>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.155G>T
  hgvsp: ENSP00000421750.1:p.Cys52Phe
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.437G>T
  hgvsp: ENSP00000264771.4:p.Cys146Phe
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.398G>T
  hgvsp: ENSP00000425181.1:p.Cys133Phe
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.89G>T
  hgvsp: ENSP00000427039.1:p.Cys30Phe
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*459G>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.1010G>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*420G>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.191G>T
  hgvsp: ENSP00000424208.1:p.Cys64Phe
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.998G>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.191G>T
  hgvsp: ENSP00000425867.1:p.Cys64Phe
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.191G>T
  hgvsp: ENSP00000423669.1:p.Cys64Phe
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.483G>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000506669
  gene symbol: TMEM175
  hgvsc: ENST00000506669.1:n.15G>T
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5982
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7734
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys146Phe
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/4-946220-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946220
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946220
    reference: chr 4
allele count: 3
allele frequency: 2.477496077297878e-5
allele num: 121090
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000506669
  gene symbol: TMEM175
  hgvsc: ENST00000506669.1:n.22C>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.198C>A
  hgvsp: ENST00000515492.1:c.198C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.1017C>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.444C>A
  hgvsp: ENST00000264771.4:c.444C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.162C>A
  hgvsp: ENST00000509508.1:c.162C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.1005C>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*466C>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*427C>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.96C>A
  hgvsp: ENST00000515740.1:c.96C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.405C>A
  hgvsp: ENST00000514453.1:c.405C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.198C>A
  hgvsp: ENST00000508204.1:c.198C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.490C>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.198C>A
  hgvsp: ENST00000510493.1:c.198C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.555C>A
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5960
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7735
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile148Ile
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-946221-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946221
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946221
    reference: chr 4
allele count: 252
allele frequency: 2.173013245033112e-3
allele num: 115968
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.1018G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.199G>A
  hgvsp: ENSP00000425867.1:p.Ala67Thr
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000506669
  gene symbol: TMEM175
  hgvsc: ENST00000506669.1:n.23G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.199G>A
  hgvsp: ENSP00000423669.1:p.Ala67Thr
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.491G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.445G>A
  hgvsp: ENSP00000264771.4:p.Ala149Thr
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.556G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.163G>A
  hgvsp: ENSP00000421750.1:p.Ala55Thr
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.97G>A
  hgvsp: ENSP00000427039.1:p.Ala33Thr
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.406G>A
  hgvsp: ENSP00000425181.1:p.Ala136Thr
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  hgvsc: ENST00000504744.1:c.*428G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.199G>A
  hgvsp: ENSP00000424208.1:p.Ala67Thr
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.1006G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*467G>A
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: missense
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7561
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5689
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 9.75e1
  variant carriers: 230
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4774
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala149Thr
num of homozygotes: 1
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP

4-946221-GCCATTGGGGTCGTGCAGGTAGGGGGCCTGGGGGGCCTGCACTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGATCA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946221
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946132
    reference: chr 4
allele count: 31
allele frequency: 2.673151214128035e-4
allele num: 115968
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000506669
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423751
  ensembl transcript: ENST00000504744
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: splice donor
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5689
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 9.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 7561
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4774
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: GCCATTGGGGTCGTGCAGGTAGGGGGCCTGGGGGGCCTGCACTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGATCA
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

4-946225-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946225
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946225
    reference: chr 4
allele count: 1
allele frequency: 8.636921110362578e-6
allele num: 115782
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.101T>G
  hgvsp: ENSP00000427039.1:p.Ile34Ser
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.1010T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*471T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.449T>G
  hgvsp: ENSP00000264771.4:p.Ile150Ser
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.560T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.167T>G
  hgvsp: ENSP00000421750.1:p.Ile56Ser
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.203T>G
  hgvsp: ENSP00000423669.1:p.Ile68Ser
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.203T>G
  hgvsp: ENSP00000424208.1:p.Ile68Ser
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.1022T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.203T>G
  hgvsp: ENSP00000425867.1:p.Ile68Ser
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.410T>G
  hgvsp: ENSP00000425181.1:p.Ile137Ser
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.495T>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000506669
  gene symbol: TMEM175
  hgvsc: ENST00000506669.1:n.27T>G
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7347
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5821
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7718
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6205
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ile150Ser
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

4-946225-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946225
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946225
    reference: chr 4
allele count: 1
allele frequency: 8.636921110362578e-6
allele num: 115782
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.167T>C
  hgvsp: ENSP00000421750.1:p.Ile56Thr
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*471T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.203T>C
  hgvsp: ENSP00000423669.1:p.Ile68Thr
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.449T>C
  hgvsp: ENSP00000264771.4:p.Ile150Thr
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.495T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.560T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.203T>C
  hgvsp: ENSP00000424208.1:p.Ile68Thr
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.410T>C
  hgvsp: ENSP00000425181.1:p.Ile137Thr
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.1010T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.1022T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000506669
  gene symbol: TMEM175
  hgvsc: ENST00000506669.1:n.27T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.203T>C
  hgvsp: ENSP00000425867.1:p.Ile68Thr
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.101T>C
  hgvsp: ENSP00000427039.1:p.Ile34Thr
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7562
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7718
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7347
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5821
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6205
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile150Thr
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

4-946226-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946226
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946226
    reference: chr 4
allele count: 1
allele frequency: 8.279105194310599e-6
allele num: 120786
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.102T>A
  hgvsp: ENST00000515740.1:c.102T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.1023T>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.1011T>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.204T>A
  hgvsp: ENST00000510493.1:c.204T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.411T>A
  hgvsp: ENST00000514453.1:c.411T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.561T>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.204T>A
  hgvsp: ENST00000515492.1:c.204T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.168T>A
  hgvsp: ENST00000509508.1:c.168T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*472T>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.496T>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000506669
  gene symbol: TMEM175
  hgvsc: ENST00000506669.1:n.28T>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.450T>A
  hgvsp: ENST00000264771.4:c.450T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.204T>A
  hgvsp: ENST00000508204.1:c.204T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44746
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile150Ile
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

4-946226-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946226
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946226
    reference: chr 4
allele count: 72042
allele frequency: 5.964432964085241e-1
allele num: 120786
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.168T>C
  hgvsp: ENST00000509508.1:c.168T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.102T>C
  hgvsp: ENST00000515740.1:c.102T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.411T>C
  hgvsp: ENST00000514453.1:c.411T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.1011T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.496T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.561T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000506669
  gene symbol: TMEM175
  hgvsc: ENST00000506669.1:n.28T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.204T>C
  hgvsp: ENST00000510493.1:c.204T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.204T>C
  hgvsp: ENST00000515492.1:c.204T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.450T>C
  hgvsp: ENST00000264771.4:c.450T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.1023T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.204T>C
  hgvsp: ENST00000508204.1:c.204T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*472T>C
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 5.75e1
  variant carriers: 359
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 3.75e1
  variant carriers: 228
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 2.75e1
  variant carriers: 215
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 7.25e1
  variant carriers: 555
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.25e1
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 136
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 9.25e1
  variant carriers: 682
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 2.25e1
  variant carriers: 181
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 5.25e1
  variant carriers: 276
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 4.75e1
  variant carriers: 230
genotype depth: GenotypeDepth
  all individuals: 44746
  bin: 9.75e1
  variant carriers: 44328
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 7.75e1
  variant carriers: 644
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 8.25e1
  variant carriers: 637
genotype quality: GenotypeQuality
hgvs: p.Ile150Ile
num of homozygotes: 21682
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

4-946226-TGGGGTCGTGCAGGTAGGGGGCCTGGGGGGCCTGCACTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGATCACCATC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946226
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946137
    reference: chr 4
allele count: 2
allele frequency: 1.65582103886212e-5
allele num: 120786
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000506669
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
reference allele: TGGGGTCGTGCAGGTAGGGGGCCTGGGGGGCCTGCACTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGATCACCATC
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ

4-946227-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946227
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946227
    reference: chr 4
allele count: 1
allele frequency: 8.672876446202148e-6
allele num: 115302
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.562G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.1024G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.205G>A
  hgvsp: ENSP00000423669.1:p.Gly69Arg
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.497G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.412G>A
  hgvsp: ENSP00000425181.1:p.Gly138Arg
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.169G>A
  hgvsp: ENSP00000421750.1:p.Gly57Arg
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.205G>A
  hgvsp: ENSP00000425867.1:p.Gly69Arg
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.205G>A
  hgvsp: ENSP00000424208.1:p.Gly69Arg
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.103G>A
  hgvsp: ENSP00000427039.1:p.Gly35Arg
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*473G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.451G>A
  hgvsp: ENSP00000264771.4:p.Gly151Arg
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000506669
  gene symbol: TMEM175
  hgvsc: ENST00000506669.1:n.29G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.1012G>A
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2825
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly151Arg
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

4-946227-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946227
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946227
    reference: chr 4
allele count: 1
allele frequency: 8.672876446202148e-6
allele num: 115302
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.412G>C
  hgvsp: ENSP00000425181.1:p.Gly138Arg
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.205G>C
  hgvsp: ENSP00000424208.1:p.Gly69Arg
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.205G>C
  hgvsp: ENSP00000423669.1:p.Gly69Arg
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*473G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.562G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.103G>C
  hgvsp: ENSP00000427039.1:p.Gly35Arg
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.1012G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.169G>C
  hgvsp: ENSP00000421750.1:p.Gly57Arg
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.451G>C
  hgvsp: ENSP00000264771.4:p.Gly151Arg
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.205G>C
  hgvsp: ENSP00000425867.1:p.Gly69Arg
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.497G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000506669
  gene symbol: TMEM175
  hgvsc: ENST00000506669.1:n.29G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.1024G>C
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2306
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly151Arg
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

4-946228-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946228
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946228
    reference: chr 4
allele count: 4
allele frequency: 3.473428273706148e-5
allele num: 115160
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.206G>C
  hgvsp: ENSP00000425867.1:p.Gly69Ala
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.206G>C
  hgvsp: ENSP00000424208.1:p.Gly69Ala
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.452G>C
  hgvsp: ENSP00000264771.4:p.Gly151Ala
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*474G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.563G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.413G>C
  hgvsp: ENSP00000425181.1:p.Gly138Ala
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.498G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.170G>C
  hgvsp: ENSP00000421750.1:p.Gly57Ala
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000506669
  gene symbol: TMEM175
  hgvsc: ENST00000506669.1:n.30G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.104G>C
  hgvsp: ENSP00000427039.1:p.Gly35Ala
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.206G>C
  hgvsp: ENSP00000423669.1:p.Gly69Ala
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.1025G>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.1013G>C
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4096
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2651
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly151Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

4-946232-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946232
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946232
    reference: chr 4
allele count: 157
allele frequency: 1.362918207545532e-3
allele num: 115194
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.1017C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*478C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.567C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.502C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.210C>T
  hgvsp: ENST00000510493.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000506669
  gene symbol: TMEM175
  hgvsc: ENST00000506669.1:n.34C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.1029C>T
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.210C>T
  hgvsp: ENST00000508204.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.417C>T
  hgvsp: ENST00000514453.1:c.417C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.456C>T
  hgvsp: ENST00000264771.4:c.456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.210C>T
  hgvsp: ENST00000515492.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.174C>T
  hgvsp: ENST00000509508.1:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.108C>T
  hgvsp: ENST00000515740.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2503
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2562
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3901
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2573
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Val152Val
num of homozygotes: 2
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum

4-946233-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946233
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946233
    reference: chr 4
allele count: 51
allele frequency: 4.427237056842251e-4
allele num: 115196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.503G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.211G>A
  hgvsp: ENSP00000423669.1:p.Val71Met
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.1030G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.109G>A
  hgvsp: ENSP00000427039.1:p.Val37Met
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.418G>A
  hgvsp: ENSP00000425181.1:p.Val140Met
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.175G>A
  hgvsp: ENSP00000421750.1:p.Val59Met
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.457G>A
  hgvsp: ENSP00000264771.4:p.Val153Met
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000506669
  gene symbol: TMEM175
  hgvsc: ENST00000506669.1:n.35G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.568G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.211G>A
  hgvsp: ENSP00000425867.1:p.Val71Met
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.211G>A
  hgvsp: ENSP00000424208.1:p.Val71Met
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*479G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.1018G>A
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2658
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2729
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3645
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3330
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22593
  bin: 9.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val153Met
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

4-946241-AGGGGGCCTG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946241
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946232
    reference: chr 4
allele count: 1
allele frequency: 8.693233187287017e-6
allele num: 115032
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000506669
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 20656
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3737
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.462+13_462+21delGGGGGCCTG
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: AGGGGGCCTG
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

4-946241-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946241
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946241
    reference: chr 4
allele count: 1
allele frequency: 8.693233187287017e-6
allele num: 115032
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.462+3A>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.216+3A>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.180+3A>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.573+3A>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.1023+3A>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.216+3A>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*484+3A>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.423+3A>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000506669
  gene symbol: TMEM175
  hgvsc: ENST00000506669.1:n.40+3A>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.1035+3A>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.508+3A>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.216+3A>G
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.114+3A>G
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 4051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3737
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.462+3A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

4-946249-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946249
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946249
    reference: chr 4
allele count: 4
allele frequency: 3.49088878028346e-5
allele num: 114584
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.1023+11T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.423+11T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.216+11T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000506669
  gene symbol: TMEM175
  hgvsc: ENST00000506669.1:n.40+11T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.573+11T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.216+11T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.114+11T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.508+11T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*484+11T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.216+11T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.462+11T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.180+11T>C
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.1035+11T>C
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1750
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2441
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23221
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2694
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

4-946250-GGGGGGCCTGCACTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGATCACCATCGGGGTCGTGCAGGTAGGGGGCCCA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946250
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946161
    reference: chr 4
allele count: 3
allele frequency: 2.617070277060507e-5
allele num: 114632
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000506669
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 22809
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3090
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1818
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2768
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: GGGGGGCCTGCACTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGATCACCATCGGGGTCGTGCAGGTAGGGGGCCCA
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

4-946254-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 946254
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 946254
    reference: chr 4
allele count: 1
allele frequency: 8.7470697316399e-6
allele num: 114324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000506669
  gene symbol: TMEM175
  hgvsc: ENST00000506669.1:n.40+16G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000438836
  gene symbol: TMEM175
  hgvsc: ENST00000438836.2:n.1023+16G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000264771
  ensembl transcript: ENST00000264771
  gene symbol: TMEM175
  hgvsc: ENST00000264771.4:c.462+16G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000452360
  gene symbol: TMEM175
  hgvsc: ENST00000452360.2:n.1035+16G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427039
  ensembl transcript: ENST00000515740
  gene symbol: TMEM175
  hgvsc: ENST00000515740.1:c.114+16G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000421750
  ensembl transcript: ENST00000509508
  gene symbol: TMEM175
  hgvsc: ENST00000509508.1:c.180+16G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000427218
  ensembl transcript: ENST00000513952
  gene symbol: TMEM175
  hgvsc: ENST00000513952.1:c.*484+16G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000424208
  ensembl transcript: ENST00000510493
  gene symbol: TMEM175
  hgvsc: ENST00000510493.1:c.216+16G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000423669
  ensembl transcript: ENST00000508204
  gene symbol: TMEM175
  hgvsc: ENST00000508204.1:c.216+16G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425181
  ensembl transcript: ENST00000514453
  gene symbol: TMEM175
  hgvsc: ENST00000514453.1:c.423+16G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000504180
  gene symbol: TMEM175
  hgvsc: ENST00000504180.1:n.508+16G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl protein: ENSP00000425867
  ensembl transcript: ENST00000515492
  gene symbol: TMEM175
  hgvsc: ENST00000515492.1:c.216+16G>A
  variant of: http://identifiers.org/hgnc/28709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000127419
  ensembl transcript: ENST00000515876
  gene symbol: TMEM175
  hgvsc: ENST00000515876.1:n.573+16G>A
  variant of: http://identifiers.org/hgnc/28709
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24047
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP

GenotypeDepth
all individuals: 3460
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2614
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2272
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4669
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4231
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2746
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 6008
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3527
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5724
bin: 9.75e1
variant carriers: 4

GenotypeDepth
all individuals: 1683
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2739
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1783
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 854
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3112
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49588
bin: 9.75e1
variant carriers: 4

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

GenotypeQuality
all individuals: 42
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1355
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1430
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1641
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 952
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1631
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.997181324777355e-5
allele num: 66698
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.268e0

MQRankSum
type: SiteQuality
SIO_000300: 6.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.72e0

DP
type: SiteQuality
SIO_000300: 3.816717e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.135e1

MQ
type: SiteQuality
SIO_000300: 5.967e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.53e-1

GenotypeDepth
all individuals: 2729
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4669
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3460
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5116
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2272
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3527
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2614
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1783
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2739
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5571
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1683
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6008
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5724
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49588
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3112
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 854
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1631
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1355
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 952
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1430
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1641
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

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

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: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66698
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.72e0

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.71e-1

QD
type: SiteQuality
SIO_000300: 1.135e1

FS
type: SiteQuality
SIO_000300: 3.268e0

DP
type: SiteQuality
SIO_000300: 3.816717e6

GenotypeDepth
all individuals: 2748
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3527
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2729
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2614
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5118
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3459
bin: 4.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 28
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2273
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2740
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1683
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5571
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5719
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3132
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1634
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1353
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 3.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 854
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1641
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49588
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 953
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1433
bin: 8.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
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: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66704
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.83e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.922e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

MQRankSum
type: SiteQuality
SIO_000300: 2.7e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.864e0

QD
type: SiteQuality
SIO_000300: 1.176e1

DP
type: SiteQuality
SIO_000300: 3.816301e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e0

GenotypeDepth
all individuals: 3527
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5718
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2273
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2750
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1785
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 5119
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4231
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2740
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 47
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2730
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5725
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1632
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3135
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1349
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49589
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 949
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1641
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 852
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1434
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.103e-1

QD
type: SiteQuality
SIO_000300: 1.124e1

MQRankSum
type: SiteQuality
SIO_000300: -1.61e-1

FS
type: SiteQuality
SIO_000300: 9.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e0

MQ
type: SiteQuality
SIO_000300: 5.89e1

DP
type: SiteQuality
SIO_000300: 3.816214e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 2273
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2740
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2745
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1683
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5118
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2623
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4670
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6008
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 60
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5718
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5725
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4231
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3137
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49589
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 46
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 949
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1348
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1641
bin: 9.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 852
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1433
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1627
bin: 6.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 1.132e1

MQ
type: SiteQuality
SIO_000300: 5.955e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.976e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.65e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.283e0

FS
type: SiteQuality
SIO_000300: 4.644e0

DP
type: SiteQuality
SIO_000300: 3.816183e6

VQSLOD
type: SiteQuality
SIO_000300: -2.848e-1

GenotypeDepth
all individuals: 4670
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6008
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2728
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 85
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4231
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1749
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1683
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5718
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5725
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1343
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49589
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 848
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1641
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 36
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 949
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3118
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1624
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1431
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.18e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.77e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.007e-1

DP
type: SiteQuality
SIO_000300: 3.815417e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e0

QD
type: SiteQuality
SIO_000300: 1.305e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.902e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 7.363e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

GenotypeDepth
all individuals: 5571
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2730
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3459
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6008
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2272
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2605
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4670
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5118
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5726
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1344
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3112
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 847
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1621
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1641
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1431
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49589
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 949
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-2

QD
type: SiteQuality
SIO_000300: 1.335e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.73e-1

DP
type: SiteQuality
SIO_000300: 3.815282e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

VQSLOD
type: SiteQuality
SIO_000300: 3.63e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.72e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.61e-1

GenotypeDepth
all individuals: 5118
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2611
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1683
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2740
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5727
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5571
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3527
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5717
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2272
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1431
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 949
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3090
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1619
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49589
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1640
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1342
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.652e0

QD
type: SiteQuality
SIO_000300: 1.324e1

DP
type: SiteQuality
SIO_000300: 3.815198e6

VQSLOD
type: SiteQuality
SIO_000300: 8.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.53e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.13e-1

MQ
type: SiteQuality
SIO_000300: 5.94e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.471e0

GenotypeDepth
all individuals: 3527
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5727
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4232
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2728
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2739
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 102
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5572
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 3460
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1683
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2736
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1615
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1640
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1343
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 846
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1431
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3092
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49591
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 949
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.028100775193798e-4
allele num: 16512
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: 66700
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.02e0

FS
type: SiteQuality
SIO_000300: 8.41e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.27e0

DP
type: SiteQuality
SIO_000300: 3.815039e6

MQRankSum
type: SiteQuality
SIO_000300: 7.76e-1

QD
type: SiteQuality
SIO_000300: 1.24e1

MQ
type: SiteQuality
SIO_000300: 5.896e1

GenotypeDepth
all individuals: 2740
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1728
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5727
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2739
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3527
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4232
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3458
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6008
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1683
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5717
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2729
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5568
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4670
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 65
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1344
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3087
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 847
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1640
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 949
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1614
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1430
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49582
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.99868058054456e-5
allele num: 66696
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.12e-1

FS
type: SiteQuality
SIO_000300: 5.679999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.375e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

VQSLOD
type: SiteQuality
SIO_000300: 8.88e-1

DP
type: SiteQuality
SIO_000300: 3.815035e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.29e-1

GenotypeDepth
all individuals: 3459
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5567
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2272
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2733
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1722
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2739
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5715
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4231
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1683
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4670
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1640
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1342
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1620
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 949
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49581
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1431
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3079
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 844
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499295331194339e-5
allele num: 66698
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.21e-1

DP
type: SiteQuality
SIO_000300: 3.814558e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.95e-1

FS
type: SiteQuality
SIO_000300: 6.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -6.038e0

VQSLOD
type: SiteQuality
SIO_000300: 5.9e-1

MQ
type: SiteQuality
SIO_000300: 5.988e1

QD
type: SiteQuality
SIO_000300: 1.379e1

GenotypeDepth
all individuals: 4670
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1702
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2273
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5119
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2730
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2742
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3458
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5727
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6007
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3527
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1344
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1431
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1640
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 844
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49581
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3032
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 949
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1615
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499295331194339e-5
allele num: 66698
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 3.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.2e-2

MQ
type: SiteQuality
SIO_000300: 5.731e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 3.814214e6

QD
type: SiteQuality
SIO_000300: 1.575e1

MQRankSum
type: SiteQuality
SIO_000300: -1.275e0

FS
type: SiteQuality
SIO_000300: 6.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.8e-2

GenotypeDepth
all individuals: 3458
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3527
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 126
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1702
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6007
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5727
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2742
bin: 8.25e1
variant carriers: 2

GenotypeDepth
all individuals: 1680
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2734
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4670
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5716
bin: 9.75e1
variant carriers: 23

GenotypeQuality
all individuals: 72
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 844
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1431
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1344
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 40
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3032
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 949
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49581
bin: 9.75e1
variant carriers: 28

GenotypeQuality
all individuals: 1615
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1640
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 28
allele frequency: 2.418797512093988e-3
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
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: 66698
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.08e0

MQ
type: SiteQuality
SIO_000300: 5.731e1

MQRankSum
type: SiteQuality
SIO_000300: -1.275e0

FS
type: SiteQuality
SIO_000300: 6.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 6.2e-2

QD
type: SiteQuality
SIO_000300: 1.575e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.64e-1

DP
type: SiteQuality
SIO_000300: 3.814214e6

GenotypeDepth
all individuals: 1681
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3527
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2271
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4670
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5119
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5727
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5567
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3458
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1615
bin: 6.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 41
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1640
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 949
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 49553
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 35
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3027
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1432
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 843
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1342
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499295331194339e-5
allele num: 66698
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 7.916e0

QD
type: SiteQuality
SIO_000300: 9.859999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -7.76e-1

DP
type: SiteQuality
SIO_000300: 3.81397e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.961e1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.465e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e0

GenotypeDepth
all individuals: 2574
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4675
bin: 4.75e1
variant carriers: 2

GenotypeDepth
all individuals: 6016
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 2732
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 5727
bin: 6.25e1
variant carriers: 2

GenotypeDepth
all individuals: 2270
bin: 8.75e1
variant carriers: 6

GenotypeDepth
all individuals: 2739
bin: 8.25e1
variant carriers: 2

GenotypeDepth
all individuals: 5700
bin: 9.75e1
variant carriers: 52

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 83
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1430
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1342
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3028
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1643
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49581
bin: 9.75e1
variant carriers: 88

GenotypeQuality
all individuals: 949
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1609
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727712508638562e-4
allele num: 11576
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 84
allele frequency: 8.087810514153668e-3
allele num: 10386
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499385252046661e-5
allele num: 66694
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.58e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

DP
type: SiteQuality
SIO_000300: 3.814224e6

FS
type: SiteQuality
SIO_000300: 5.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.592e0

MQRankSum
type: SiteQuality
SIO_000300: 1.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

QD
type: SiteQuality
SIO_000300: 1.297e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 2572
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2740
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5124
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 1.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2737
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1678
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6021
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1435
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1343
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1643
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 46
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49563
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 949
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1607
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3019
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49934029027228e-5
allele num: 66696
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.77e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.951000000000001e-1

FS
type: SiteQuality
SIO_000300: 9.276999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 2.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.0e-2

MQ
type: SiteQuality
SIO_000300: 5.949e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 3.809643e6

QD
type: SiteQuality
SIO_000300: 9.01e0

GenotypeDepth
all individuals: 5574
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6021
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3473
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4229
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2737
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5667
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3527
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1678
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 949
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1333
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2849
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1577
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49558
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1641
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1426
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
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: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499745043342632e-5
allele num: 66678
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e-1

FS
type: SiteQuality
SIO_000300: 1.109e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 3.807978e6

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

VQSLOD
type: SiteQuality
SIO_000300: 5.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.669e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.73e-1

QD
type: SiteQuality
SIO_000300: 1.218e1

GenotypeDepth
all individuals: 5569
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1677
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4228
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5666
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5731
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6020
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2718
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2266
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 942
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 804
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1451
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2385
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49553
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 126
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1315
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1638
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1425
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.592912705272256e-4
allele num: 11570
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66666
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: 16508
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.88e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.034e0

VQSLOD
type: SiteQuality
SIO_000300: 4.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.59e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

QD
type: SiteQuality
SIO_000300: 1.188e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 3.803343e6

GenotypeDepth
all individuals: 2688
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 520
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1249
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4615
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 917
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 685
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36515
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2956
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 726
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2967
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 679
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1964
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1921
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2999
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2842
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4364
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10226
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52452968259292e-5
allele num: 65594
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: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.735e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.72e-1

QD
type: SiteQuality
SIO_000300: 1.628e1

DP
type: SiteQuality
SIO_000300: 2.646759e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: -9.67e-1

FS
type: SiteQuality
SIO_000300: 5.976e0

MQRankSum
type: SiteQuality
SIO_000300: 3.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-1

GenotypeDepth
all individuals: 685
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5018
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1885
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 520
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5053
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1281
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3045
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5009
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36522
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 743
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1964
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2993
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2869
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3005
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1945
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.079766536964981e-5
allele num: 16448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65628
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10232
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8402
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.121e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.55e0

MQRankSum
type: SiteQuality
SIO_000300: -2.84e-1

MQ
type: SiteQuality
SIO_000300: 5.839e1

DP
type: SiteQuality
SIO_000300: 2.654268e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.078e1

VQSLOD
type: SiteQuality
SIO_000300: -2.702e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.331e0

GenotypeDepth
all individuals: 405
bin: 9.25e1
variant carriers: 2

GenotypeDepth
all individuals: 805
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1283
bin: 7.25e1
variant carriers: 2

GenotypeDepth
all individuals: 7519
bin: 4.25e1
variant carriers: 7

GenotypeDepth
all individuals: 686
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3680
bin: 5.75e1
variant carriers: 7

GenotypeQuality
all individuals: 135
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3038
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3035
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2970
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5541
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1993
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36608
bin: 9.75e1
variant carriers: 58

GenotypeQuality
all individuals: 249
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1988
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3184
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 55
allele frequency: 5.366900858704137e-3
allele num: 10248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.041085059149104e-5
allele num: 65766
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8460
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
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: 1
allele frequency: 8.674531575294934e-5
allele num: 11528
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.579e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.88e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.95e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.95e0

MQ
type: SiteQuality
SIO_000300: 5.835e1

VQSLOD
type: SiteQuality
SIO_000300: 8.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.92e-1

DP
type: SiteQuality
SIO_000300: 2.670116e6

GenotypeDepth
all individuals: 3682
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1374
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 685
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 7551
bin: 4.25e1
variant carriers: 2

GenotypeDepth
all individuals: 927
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1292
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 101
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 98
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 241
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 361
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 577
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3030
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 58
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 63
bin: 1.25e1
variant carriers: 5

GenotypeQuality
all individuals: 188
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3039
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36556
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 5512
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 155
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1985
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3161
bin: 6.75e1
variant carriers: 6

GenotypeQuality
all individuals: 157
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 2937
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8462
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 6.862745098039216e-4
allele num: 10200
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 21
allele frequency: 3.20786997433704e-4
allele num: 65464
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.677542519958348e-5
allele num: 11524
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.215066828675577e-4
allele num: 16460
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 9.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.57e-1

QD
type: SiteQuality
SIO_000300: 8.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.06e-1

MQ
type: SiteQuality
SIO_000300: 5.714e1

DP
type: SiteQuality
SIO_000300: 2.677937e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 927
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5386
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1374
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1292
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5044
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 685
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5512
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3161
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1985
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36556
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 101
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2937
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3039
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3030
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527557130636686e-5
allele num: 65464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10200
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.57e-1

MQ
type: SiteQuality
SIO_000300: 5.714e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.3e-1

QD
type: SiteQuality
SIO_000300: 8.5e-1

DP
type: SiteQuality
SIO_000300: 2.677937e6

GenotypeDepth
all individuals: 326
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2702
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1894
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5054
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 409
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 548
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1997
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3038
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3047
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36611
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3190
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2949
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5649
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1992
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10248
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8462
num of homozygotes: 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: 1
allele frequency: 1.521838380763963e-5
allele num: 65710
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.516e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQ
type: SiteQuality
SIO_000300: 5.848e1

DP
type: SiteQuality
SIO_000300: 2.681655e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.562e0

FS
type: SiteQuality
SIO_000300: 5.941e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

QD
type: SiteQuality
SIO_000300: 1.595e1

GenotypeDepth
all individuals: 525
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6488
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 690
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 409
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1295
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7578
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5775
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2023
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2990
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2017
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 535
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3071
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36720
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3240
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3080
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65984
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: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.553e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.9e-1

QD
type: SiteQuality
SIO_000300: 1.236e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.117e0

FS
type: SiteQuality
SIO_000300: 1.319e0

DP
type: SiteQuality
SIO_000300: 2.684417e6

VQSLOD
type: SiteQuality
SIO_000300: -1.339e0

MQ
type: SiteQuality
SIO_000300: 5.786e1

GenotypeDepth
all individuals: 3689
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 525
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7578
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 690
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 922
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6488
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3080
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2017
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5775
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3240
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36720
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2990
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 86
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2023
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3071
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 2.75e1
variant carriers: 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: 6590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.072382803011902e-5
allele num: 16468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65984
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.9e-1

DP
type: SiteQuality
SIO_000300: 2.684417e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

QD
type: SiteQuality
SIO_000300: 1.236e1

MQRankSum
type: SiteQuality
SIO_000300: 2.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.553e0

VQSLOD
type: SiteQuality
SIO_000300: -1.339e0

FS
type: SiteQuality
SIO_000300: 1.319e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.117e0

MQ
type: SiteQuality
SIO_000300: 5.786e1

GenotypeDepth
all individuals: 7960
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 691
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1376
bin: 9.75e1
variant carriers: 3

GenotypeDepth
all individuals: 410
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 526
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1895
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 79
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36790
bin: 9.75e1
variant carriers: 20

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

GenotypeQuality
all individuals: 2054
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2073
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3131
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3048
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3294
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5936
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3109
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.337540906965872e-4
allele num: 8556
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.733102253032929e-4
allele num: 11540
num of homozygotes: 0

African
type: Population
allele count: 16
allele frequency: 1.552192471866511e-3
allele num: 10308
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66134
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.692167e6

MQ
type: SiteQuality
SIO_000300: 5.8e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 9.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.54e0

MQRankSum
type: SiteQuality
SIO_000300: 2.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.79e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.186e-1

QD
type: SiteQuality
SIO_000300: 1.364e1

GenotypeDepth
all individuals: 1378
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 692
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 922
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 526
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 409
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1896
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2103
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3364
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3115
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2068
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3072
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3147
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36800
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6214
bin: 6.25e1
variant carriers: 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: 11542
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.693679720822024e-5
allele num: 10316
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510072181450273e-5
allele num: 66222
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.166044776119403e-4
allele num: 8576
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.705e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

FS
type: SiteQuality
SIO_000300: 1.736e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.119e0

VQSLOD
type: SiteQuality
SIO_000300: -1.277e0

QD
type: SiteQuality
SIO_000300: 1.025e1

DP
type: SiteQuality
SIO_000300: 2.695684e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.618e0

GenotypeDepth
all individuals: 7613
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3698
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2713
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 410
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6510
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1380
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 30
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3399
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3122
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6381
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36817
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3092
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2079
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3159
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2117
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
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: 1
allele frequency: 1.507704369327262e-5
allele num: 66326
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.14e-1

FS
type: SiteQuality
SIO_000300: 1.639e0

MQ
type: SiteQuality
SIO_000300: 5.35e1

VQSLOD
type: SiteQuality
SIO_000300: 1.98e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.56e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.604e0

QD
type: SiteQuality
SIO_000300: 8.640000000000001e0

DP
type: SiteQuality
SIO_000300: 2.699362e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-2

GenotypeDepth
all individuals: 128
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1299
bin: 7.25e1
variant carriers: 2

GenotypeDepth
all individuals: 701
bin: 8.25e1
variant carriers: 10

GenotypeDepth
all individuals: 535
bin: 8.75e1
variant carriers: 8

GenotypeDepth
all individuals: 925
bin: 7.75e1
variant carriers: 5

GenotypeDepth
all individuals: 415
bin: 9.25e1
variant carriers: 6

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3406
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3159
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2078
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36855
bin: 9.75e1
variant carriers: 116

GenotypeQuality
all individuals: 3117
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2120
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6407
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3098
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 116
allele frequency: 1.347270615563298e-2
allele num: 8610
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66364
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 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: 902
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.01e-1

MQ
type: SiteQuality
SIO_000300: 5.774e1

MQRankSum
type: SiteQuality
SIO_000300: 6.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.15e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.509e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.13e-2

DP
type: SiteQuality
SIO_000300: 2.707526e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.18e-1

GenotypeDepth
all individuals: 532
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5917
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 702
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 924
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1300
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7606
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3412
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2120
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3097
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3118
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3161
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6428
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2079
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36856
bin: 9.75e1
variant carriers: 1

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
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: 1.506750241080039e-5
allele num: 66368
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.67e0

VQSLOD
type: SiteQuality
SIO_000300: -2.336e0

FS
type: SiteQuality
SIO_000300: 1.395e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.634e0

DP
type: SiteQuality
SIO_000300: 2.708067e6

QD
type: SiteQuality
SIO_000300: 1.717e1

MQ
type: SiteQuality
SIO_000300: 5.712e1

GenotypeDepth
all individuals: 7610
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 532
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1895
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1446
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 705
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 415
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3099
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3411
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36852
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3158
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6418
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2078
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2120
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3117
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 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: 11566
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: 1
allele frequency: 1.50665943470138e-5
allele num: 66372
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.89e0

MQRankSum
type: SiteQuality
SIO_000300: -1.048e0

DP
type: SiteQuality
SIO_000300: 2.708527e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-1

QD
type: SiteQuality
SIO_000300: 1.615e1

FS
type: SiteQuality
SIO_000300: 3.543e0

VQSLOD
type: SiteQuality
SIO_000300: -1.381e0

MQ
type: SiteQuality
SIO_000300: 5.745e1

GenotypeDepth
all individuals: 5054
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 925
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 703
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 416
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6492
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1300
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1895
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6011
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2077
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6492
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3413
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3169
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3117
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36863
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2131
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3106
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.67305088024763e-5
allele num: 10338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66440
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.231e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

FS
type: SiteQuality
SIO_000300: 2.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.261e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.91e0

DP
type: SiteQuality
SIO_000300: 2.710187e6

MQ
type: SiteQuality
SIO_000300: 5.756e1

VQSLOD
type: SiteQuality
SIO_000300: -1.743e0

GenotypeDepth
all individuals: 7716
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 167
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2710
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1895
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 925
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1300
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7969
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 175
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6534
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 36865
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3423
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3171
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2077
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3119
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3109
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2129
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503804625703029e-5
allele num: 66498
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: 8634
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.775e0

DP
type: SiteQuality
SIO_000300: 2.711249e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.676e0

MQRankSum
type: SiteQuality
SIO_000300: 6.35e-1

QD
type: SiteQuality
SIO_000300: 1.52e1

MQ
type: SiteQuality
SIO_000300: 5.76e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.259e0

GenotypeDepth
all individuals: 6493
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 416
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7967
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1895
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1453
bin: 9.75e1
variant carriers: 3

GenotypeDepth
all individuals: 5054
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 534
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3173
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6555
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3111
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2130
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3120
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36866
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 167
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2077
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3429
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

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

African
type: Population
allele count: 5
allele frequency: 4.834654805646877e-4
allele num: 10342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66510
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.738e1

VQSLOD
type: SiteQuality
SIO_000300: 5.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.97e-1

DP
type: SiteQuality
SIO_000300: 2.712023e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.31e0

QD
type: SiteQuality
SIO_000300: 1.304e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e-1

GenotypeDepth
all individuals: 116
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3692
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1896
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 534
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2710
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3115
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6569
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36867
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2079
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3446
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3122
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3173
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2142
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66580
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.659969088098918e-5
allele num: 10352
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.876e0

QD
type: SiteQuality
SIO_000300: 1.361e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 9.65e-1

MQ
type: SiteQuality
SIO_000300: 5.809e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.134e0

MQRankSum
type: SiteQuality
SIO_000300: 1.98e0

DP
type: SiteQuality
SIO_000300: 2.713367e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.163e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e0

GenotypeDepth
all individuals: 1896
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 534
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1299
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5054
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1454
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2140
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6560
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3122
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2078
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36868
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3175
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3448
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3115
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66580
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -4.117e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.353e0

DP
type: SiteQuality
SIO_000300: 2.713533e6

FS
type: SiteQuality
SIO_000300: 6.929999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.058e0

MQRankSum
type: SiteQuality
SIO_000300: 1.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.223e1

MQ
type: SiteQuality
SIO_000300: 5.784e1

GenotypeDepth
all individuals: 416
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1896
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1455
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 7740
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2710
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3447
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 127
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3115
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2079
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3124
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6539
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36869
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2142
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3179
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
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: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50177209106746e-5
allele num: 66588
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.601e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.713715e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.29e0

QD
type: SiteQuality
SIO_000300: 1.247e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.368e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.63e0

MQ
type: SiteQuality
SIO_000300: 5.681e1

GenotypeDepth
all individuals: 3692
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1456
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1299
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 925
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7743
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3121
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2141
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3438
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3114
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6535
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36871
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2080
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3176
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50159168718842e-5
allele num: 66596
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: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.544e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.091e0

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.249e0

QD
type: SiteQuality
SIO_000300: 1.806e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.866e0

MQ
type: SiteQuality
SIO_000300: 5.749e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.713964e6

GenotypeDepth
all individuals: 1457
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 7972
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2710
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 534
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6493
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 134
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36870
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3437
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2140
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6535
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3121
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3177
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3114
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2079
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50159168718842e-5
allele num: 66596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
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: 902
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.62e-1

FS
type: SiteQuality
SIO_000300: 5.570000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.714032e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.016e0

MQ
type: SiteQuality
SIO_000300: 5.379e1

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

QD
type: SiteQuality
SIO_000300: 2.216e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.01e-1

GenotypeDepth
all individuals: 5054
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 703
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3692
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 925
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 65
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6493
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 534
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1461
bin: 9.75e1
variant carriers: 4

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

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3112
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6527
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2079
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3179
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 137
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3441
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3120
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2140
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36871
bin: 9.75e1
variant carriers: 4

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66598
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: 4
allele frequency: 4.627487274409995e-4
allele num: 8644
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 10358
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.812e0

VQSLOD
type: SiteQuality
SIO_000300: -1.051e0

MQRankSum
type: SiteQuality
SIO_000300: 4.75e-1

QD
type: SiteQuality
SIO_000300: 1.4e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.714704e6

MQ
type: SiteQuality
SIO_000300: 5.728e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.272e0

GenotypeDepth
all individuals: 534
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7970
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7611
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 925
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1465
bin: 9.75e1
variant carriers: 4

GenotypeDepth
all individuals: 6492
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1298
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3112
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6520
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2079
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3434
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2135
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36873
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 3121
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3176
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66598
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.627487274409995e-4
allele num: 8644
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: 10354
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.712e1

FS
type: SiteQuality
SIO_000300: 1.104e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.051e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.295e0

VQSLOD
type: SiteQuality
SIO_000300: -2.071e0

DP
type: SiteQuality
SIO_000300: 2.715084e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.387e1

GenotypeDepth
all individuals: 936
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6491
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1311
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7617
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 544
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5049
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6425
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3117
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36880
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 40
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3404
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3164
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2078
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2116
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3094
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
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: 6610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504392827055001e-5
allele num: 66472
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.97e-1

MQ
type: SiteQuality
SIO_000300: 5.74e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.14e0

MQRankSum
type: SiteQuality
SIO_000300: 4.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.87e-1

QD
type: SiteQuality
SIO_000300: 1.185e1

DP
type: SiteQuality
SIO_000300: 2.736501e6

GenotypeDepth
all individuals: 6491
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5966
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5879
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 718
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7965
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 544
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3688
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3094
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36880
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2116
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2078
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6425
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3117
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 140
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3164
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3404
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 4
allele frequency: 3.867723844517501e-4
allele num: 10342
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66472
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

DP
type: SiteQuality
SIO_000300: 2.736501e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.87e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.03e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

MQ
type: SiteQuality
SIO_000300: 5.74e1

QD
type: SiteQuality
SIO_000300: 1.185e1

GenotypeDepth
all individuals: 2708
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1311
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1903
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3688
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 6491
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1550
bin: 9.75e1
variant carriers: 7

GenotypeDepth
all individuals: 718
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 544
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36880
bin: 9.75e1
variant carriers: 7

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

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

GenotypeQuality
all individuals: 6425
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 40
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 74
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 2078
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3404
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 3094
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2116
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3164
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3117
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.026356962330004e-5
allele num: 66472
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.789717461787865e-4
allele num: 8636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.062810719049351e-5
allele num: 16494
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.74e1

VQSLOD
type: SiteQuality
SIO_000300: 5.14e0

QD
type: SiteQuality
SIO_000300: 1.185e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.87e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

DP
type: SiteQuality
SIO_000300: 2.736501e6

GenotypeDepth
all individuals: 85
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 935
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1307
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2712
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7611
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 539
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5050
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5972
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 80
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3117
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6416
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3096
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3162
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2078
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3405
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2117
bin: 7.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 36911
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 35
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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: 11564
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504347564461293e-5
allele num: 66474
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.24e-1

MQ
type: SiteQuality
SIO_000300: 5.723e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.03e-1

FS
type: SiteQuality
SIO_000300: 5.18e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.138e0

QD
type: SiteQuality
SIO_000300: 1.266e1

DP
type: SiteQuality
SIO_000300: 2.736155e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeDepth
all individuals: 7611
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 540
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2711
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5823
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5051
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 715
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 82
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1543
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3168
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 128
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 57
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2120
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3104
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6426
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3413
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2078
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36925
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3119
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
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: 16506
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50271992306074e-5
allele num: 66546
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: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.309e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.84e-1

MQ
type: SiteQuality
SIO_000300: 5.782e1

QD
type: SiteQuality
SIO_000300: 1.025e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.684e0

FS
type: SiteQuality
SIO_000300: 2.322e0

VQSLOD
type: SiteQuality
SIO_000300: -1.711e0

MQRankSum
type: SiteQuality
SIO_000300: -7.78e-1

DP
type: SiteQuality
SIO_000300: 2.735612e6

GenotypeDepth
all individuals: 3696
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1910
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 539
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5801
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 935
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7958
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7615
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 423
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 38
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3116
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6312
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3163
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3102
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2079
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3408
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36921
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2111
bin: 7.25e1
variant carriers: 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: 8638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.509786236132407e-5
allele num: 66522
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.6e-2

DP
type: SiteQuality
SIO_000300: 2.736813e6

QD
type: SiteQuality
SIO_000300: 1.02e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.618e1

VQSLOD
type: SiteQuality
SIO_000300: -3.887e-1

FS
type: SiteQuality
SIO_000300: 1.778e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.36e-1

GenotypeDepth
all individuals: 3448
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1721
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5815
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6202
bin: 4.75e1
variant carriers: 2

GenotypeDepth
all individuals: 7718
bin: 3.75e1
variant carriers: 2

GenotypeDepth
all individuals: 795
bin: 7.75e1
variant carriers: 3

GenotypeDepth
all individuals: 7347
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 609
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 132
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3036
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2030
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3327
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2345
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2078
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3090
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3027
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6154
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34801
bin: 9.75e1
variant carriers: 251

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 35
allele frequency: 5.652454780361757e-3
allele num: 6192
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 6.109979633401223e-4
allele num: 9820
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.252100840336134e-4
allele num: 11424
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 205
allele frequency: 3.266619924788068e-3
allele num: 62756
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.69e-1

QD
type: SiteQuality
SIO_000300: 1.44e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.35e0

MQ
type: SiteQuality
SIO_000300: 5.703e1

FS
type: SiteQuality
SIO_000300: 4.115e0

VQSLOD
type: SiteQuality
SIO_000300: -1.549e0

DP
type: SiteQuality
SIO_000300: 3.291983e6

GenotypeDepth
all individuals: 6202
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1721
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5815
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 460
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 363
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7347
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7718
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 609
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3448
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2078
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3090
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 84
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 132
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3027
bin: 7.75e1
variant carriers: 4

GenotypeQuality
all individuals: 53
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 34801
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2345
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 67
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 3036
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6154
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2030
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3327
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 6

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.39020970106444e-4
allele num: 62756
num of homozygotes: 0

African
type: Population
allele count: 12
allele frequency: 1.221995926680245e-3
allele num: 9820
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.102770657878677e-5
allele num: 16386
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.229974160206718e-4
allele num: 6192
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.753501400560224e-5
allele num: 11424
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.7e-2

MQ
type: SiteQuality
SIO_000300: 5.703e1

FS
type: SiteQuality
SIO_000300: 4.115e0

QD
type: SiteQuality
SIO_000300: 1.44e0

VQSLOD
type: SiteQuality
SIO_000300: -1.549e0

DP
type: SiteQuality
SIO_000300: 3.291983e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.96e-1

GenotypeDepth
all individuals: 3450
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 457
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1719
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7562
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 131
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6103
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2023
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2068
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 78
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2359
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3024
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34799
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3317
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3085
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3038
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.021450459652707e-4
allele num: 9790
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62632
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6184
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.34e-1

DP
type: SiteQuality
SIO_000300: 3.271044e6

VQSLOD
type: SiteQuality
SIO_000300: -1.142e0

FS
type: SiteQuality
SIO_000300: 7.118e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

MQ
type: SiteQuality
SIO_000300: 5.666e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.22e0

MQRankSum
type: SiteQuality
SIO_000300: 9.48e-1

QD
type: SiteQuality
SIO_000300: 1.422e1

GenotypeDepth
all individuals: 797
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2514
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3892
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 366
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 609
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3038
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3024
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3317
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2068
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6103
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2359
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2023
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3085
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34799
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6184
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.021450459652707e-4
allele num: 9790
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62632
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.22e0

MQ
type: SiteQuality
SIO_000300: 5.666e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.422e1

FS
type: SiteQuality
SIO_000300: 7.118e0

MQRankSum
type: SiteQuality
SIO_000300: 9.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.34e-1

DP
type: SiteQuality
SIO_000300: 3.271044e6

VQSLOD
type: SiteQuality
SIO_000300: -1.142e0

GenotypeDepth
all individuals: 817
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1543
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 951
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 752
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 739
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1350
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55334
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508068164681044e-5
allele num: 66310
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.69e-1

DP
type: SiteQuality
SIO_000300: 9.493369e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.12e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.34e0

FS
type: SiteQuality
SIO_000300: 5.23e-1

QD
type: SiteQuality
SIO_000300: 2.066e1

MQ
type: SiteQuality
SIO_000300: 5.733e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.0e-3

GenotypeDepth
all individuals: 1565
bin: 4.25e1
variant carriers: 244

GenotypeDepth
all individuals: 796
bin: 6.25e1
variant carriers: 342

GenotypeDepth
all individuals: 817
bin: 6.75e1
variant carriers: 457

GenotypeDepth
all individuals: 1480
bin: 3.25e1
variant carriers: 225

GenotypeDepth
all individuals: 739
bin: 8.75e1
variant carriers: 637

GenotypeQuality
all individuals: 589
bin: 9.25e1
variant carriers: 68

GenotypeQuality
all individuals: 424
bin: 8.75e1
variant carriers: 71

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 47

GenotypeQuality
all individuals: 71
bin: 2.25e1
variant carriers: 27

GenotypeQuality
all individuals: 63
bin: 3.75e1
variant carriers: 59

GenotypeQuality
all individuals: 659
bin: 6.75e1
variant carriers: 76

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 28

GenotypeQuality
all individuals: 55
bin: 4.75e1
variant carriers: 50

GenotypeQuality
all individuals: 38
bin: 1.25e1
variant carriers: 33

GenotypeQuality
all individuals: 1350
bin: 6.25e1
variant carriers: 70

GenotypeQuality
all individuals: 159
bin: 2.5e0
variant carriers: 28

GenotypeQuality
all individuals: 37
bin: 7.5e0
variant carriers: 34

GenotypeQuality
all individuals: 49
bin: 2.75e1
variant carriers: 40

GenotypeQuality
all individuals: 63
bin: 3.25e1
variant carriers: 52

GenotypeQuality
all individuals: 55334
bin: 9.75e1
variant carriers: 49529

GenotypeQuality
all individuals: 580
bin: 7.75e1
variant carriers: 55

GenotypeQuality
all individuals: 431
bin: 7.25e1
variant carriers: 62

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 45

GenotypeQuality
all individuals: 599
bin: 8.25e1
variant carriers: 79

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 55

Latino
type: Population
allele count: 4771
allele frequency: 4.132166984236965e-1
allele num: 11546
num of homozygotes: 1023

East Asian
type: Population
allele count: 6292
allele frequency: 7.309479553903345e-1
allele num: 8608
num of homozygotes: 2314

European (Finnish)
type: Population
allele count: 3424
allele frequency: 5.19890677194048e-1
allele num: 6586
num of homozygotes: 884

African
type: Population
allele count: 7403
allele frequency: 7.16234520123839e-1
allele num: 10336
num of homozygotes: 2621

South Asian
type: Population
allele count: 10526
allele frequency: 6.38094083414161e-1
allele num: 16496
num of homozygotes: 3409

European (Non-Finnish)
type: Population
allele count: 39076
allele frequency: 5.892927160307646e-1
allele num: 66310
num of homozygotes: 11263

Other
type: Population
allele count: 550
allele frequency: 6.084070796460177e-1
allele num: 904
num of homozygotes: 168

ClippingRankSum
type: SiteQuality
SIO_000300: -5.69e-1

DP
type: SiteQuality
SIO_000300: 9.493369e6

FS
type: SiteQuality
SIO_000300: 5.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.12e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.34e0

MQRankSum
type: SiteQuality
SIO_000300: 4.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.16e-1

MQ
type: SiteQuality
SIO_000300: 5.733e1

QD
type: SiteQuality
SIO_000300: 2.066e1

GenotypeDepth
all individuals: 752
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 817
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1480
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 759
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1565
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 44746
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1543
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1350
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55334
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508068164681044e-5
allele num: 66310
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.674922600619196e-5
allele num: 10336
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: 16496
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.12e-2

FS
type: SiteQuality
SIO_000300: 5.23e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.08e-1

DP
type: SiteQuality
SIO_000300: 9.493369e6

VQSLOD
type: SiteQuality
SIO_000300: 3.34e0

QD
type: SiteQuality
SIO_000300: 2.066e1

MQ
type: SiteQuality
SIO_000300: 5.733e1

GenotypeDepth
all individuals: 3288
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1674
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2988
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24406
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2306
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1366
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2328
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1129
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 948
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2277
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4947
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1633
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43368
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1494
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6154
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62296
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.027960526315789e-4
allele num: 9728
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16370
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8496
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.62e-1

DP
type: SiteQuality
SIO_000300: 5.348339e6

FS
type: SiteQuality
SIO_000300: 1.743e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.77e-1

QD
type: SiteQuality
SIO_000300: 1.434e1

MQ
type: SiteQuality
SIO_000300: 5.881e1

GenotypeDepth
all individuals: 3288
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 96
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1674
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2825
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24406
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2328
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43368
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1633
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1494
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2277
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1129
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1366
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 948
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4947
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9728
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.605239501733659e-5
allele num: 62296
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6154
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16370
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.743e0

MQ
type: SiteQuality
SIO_000300: 5.881e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e0

DP
type: SiteQuality
SIO_000300: 5.348339e6

QD
type: SiteQuality
SIO_000300: 1.434e1

MQRankSum
type: SiteQuality
SIO_000300: 8.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

GenotypeDepth
all individuals: 19021
bin: 9.75e1
variant carriers: 4

GenotypeDepth
all individuals: 2025
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4243
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2258
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1993
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2470
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2584
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5203
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1785
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1932
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2016
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40976
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1347
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1231
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.791981712678038e-5
allele num: 11374
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16314
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.210272873194221e-5
allele num: 62300
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9704
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.622849724115547e-4
allele num: 6162
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8452
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.340000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.12e-1

DP
type: SiteQuality
SIO_000300: 4.82828e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.114e0

MQ
type: SiteQuality
SIO_000300: 5.762e1

QD
type: SiteQuality
SIO_000300: 1.259e1

FS
type: SiteQuality
SIO_000300: 5.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

MQRankSum
type: SiteQuality
SIO_000300: 4.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.78e-1

GenotypeDepth
all individuals: 2301
bin: 7.75e1
variant carriers: 4

GenotypeDepth
all individuals: 2937
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2128
bin: 7.25e1
variant carriers: 5

GenotypeDepth
all individuals: 21609
bin: 9.75e1
variant carriers: 115

GenotypeDepth
all individuals: 1904
bin: 6.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 2357
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1589
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42180
bin: 9.75e1
variant carriers: 155

GenotypeQuality
all individuals: 1816
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1698
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 30
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4974
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2448
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1239
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1116
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.423226386613996e-5
allele num: 62274
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.390586582367404e-4
allele num: 11388
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.223840411210378e-4
allele num: 16342
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.626545217957059e-4
allele num: 6148
num of homozygotes: 0

African
type: Population
allele count: 145
allele frequency: 1.493305870236869e-2
allele num: 9710
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8478
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.071385e6

VQSLOD
type: SiteQuality
SIO_000300: 1.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.64e0

QD
type: SiteQuality
SIO_000300: 1.435e1

MQ
type: SiteQuality
SIO_000300: 5.743e1

MQRankSum
type: SiteQuality
SIO_000300: 8.06e-1

GenotypeDepth
all individuals: 1840
bin: 6.25e1
variant carriers: 2

GenotypeDepth
all individuals: 2385
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2161
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2683
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3281
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1483
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 41
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4902
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2382
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2309
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1741
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1051
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1643
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1194
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42608
bin: 9.75e1
variant carriers: 51

Latino
type: Population
allele count: 1
allele frequency: 8.775008775008775e-5
allele num: 11396
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16366
num of homozygotes: 0

African
type: Population
allele count: 49
allele frequency: 5.045304777594728e-3
allele num: 9712
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6142
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.606683804627249e-5
allele num: 62240
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.847e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.7e-2

QD
type: SiteQuality
SIO_000300: 1.43e1

DP
type: SiteQuality
SIO_000300: 5.160403e6

MQRankSum
type: SiteQuality
SIO_000300: 4.91e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.409999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.299999999999999e-3

MQ
type: SiteQuality
SIO_000300: 5.712e1

GenotypeDepth
all individuals: 45
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2017
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1931
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 85
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2356
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4791
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1882
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41756
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2427
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1118
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1652
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1284
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1763
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.030290541932825e-4
allele num: 9706
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6140
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11374
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62130
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16346
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 4.71e0

VQSLOD
type: SiteQuality
SIO_000300: 4.38e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.38e-1

DP
type: SiteQuality
SIO_000300: 4.969094e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.012e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.7e-3

FS
type: SiteQuality
SIO_000300: 1.758e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

MQ
type: SiteQuality
SIO_000300: 5.445e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.156e0

GenotypeDepth
all individuals: 1759
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2275
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2479
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 300
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2017
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 154
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 20656
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 535
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2356
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41756
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1763
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1284
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1882
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2427
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1652
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4791
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1118
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.609528408176404e-5
allele num: 62130
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9706
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6140
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11374
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16346
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.7e-3

FS
type: SiteQuality
SIO_000300: 1.758e0

MQRankSum
type: SiteQuality
SIO_000300: -2.38e-1

QD
type: SiteQuality
SIO_000300: 4.71e0

DP
type: SiteQuality
SIO_000300: 4.969094e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.156e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.012e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

MQ
type: SiteQuality
SIO_000300: 5.445e1

GenotypeDepth
all individuals: 236
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2560
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2273
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4419
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 958
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1080
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2431
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1400
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1571
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2128
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42807
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1458
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6130
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.809020436927414e-5
allele num: 11352
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16358
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.110097449720091e-4
allele num: 9646
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61804
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.3e-1

FS
type: SiteQuality
SIO_000300: 8.581e0

DP
type: SiteQuality
SIO_000300: 5.205731e6

VQSLOD
type: SiteQuality
SIO_000300: -1.049e0

QD
type: SiteQuality
SIO_000300: 1.063e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.07e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

MQ
type: SiteQuality
SIO_000300: 5.596e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.58e-1

GenotypeQuality
all individuals: 2148
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 273
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1452
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1105
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 44
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2407
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4481
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 227
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 976
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1526
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1605
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42627
bin: 9.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9670
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11356
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6130
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.234048057954141e-5
allele num: 61842
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.11545988258317e-5
allele num: 16352
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.16602e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.06e-1

QD
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.05e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.02e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.54e-1

MQ
type: SiteQuality
SIO_000300: 5.651e1

FS
type: SiteQuality
SIO_000300: 4.232e0

VQSLOD
type: SiteQuality
SIO_000300: -9.531000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.324e0

GenotypeDepth
all individuals: 1367
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1697
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2505
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 918
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1391
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1965
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2430
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 719
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1015
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1514
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1356
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3783
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43137
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16344
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8432
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.62295507660348e-5
allele num: 61616
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11338
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6130
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.05e-2

DP
type: SiteQuality
SIO_000300: 5.279883e6