19-37643463-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643463
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643463
    reference: chr 19
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3304G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.1173G>C
  hgvsp: ENSP00000375998.1:p.Leu391Phe
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1338G>C
  hgvsp: ENSP00000349440.2:p.Leu446Phe
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+235G>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1682G>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.1173G>C
  hgvsp: ENSP00000292841.5:p.Leu391Phe
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3304G>C
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38140
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12921
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3080
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1967
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41845
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6936
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu391Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

19-37643470-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643470
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643470
    reference: chr 19
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.1166G>A
  hgvsp: ENSP00000375998.1:p.Gly389Glu
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1331G>A
  hgvsp: ENSP00000349440.2:p.Gly444Glu
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.1166G>A
  hgvsp: ENSP00000292841.5:p.Gly389Glu
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3297G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1689G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3297G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+228G>A
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12924
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1967
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2648
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6936
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41809
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gly389Glu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/19-37643471-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643471
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643471
    reference: chr 19
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.1165G>T
  hgvsp: ENSP00000292841.5:p.Gly389Trp
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.1165G>T
  hgvsp: ENSP00000375998.1:p.Gly389Trp
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+227G>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1330G>T
  hgvsp: ENSP00000349440.2:p.Gly444Trp
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3296G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3296G>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1690G>T
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12924
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41814
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6936
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly389Trp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQ

19-37643472-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643472
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643472
    reference: chr 19
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.1164T>C
  hgvsp: ENST00000392157.2:c.1164T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1691T>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1329T>C
  hgvsp: ENST00000356958.4:c.1329T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+226T>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3295T>C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.1164T>C
  hgvsp: ENST00000292841.5:c.1164T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3295T>C
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12924
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3080
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2648
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2760
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Cys388Cys
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: A
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

19-37643477-GACC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643477
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643474
    reference: chr 19
allele count: 5
allele frequency: 4.118819711023609e-5
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1699_293-1697delGGT
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3287_502+3289delGGT
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+218_938+220delGGT
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.1156_1158delGGT
  hgvsp: ENSP00000292841.5:p.Gly386del
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1321_1323delGGT
  hgvsp: ENSP00000349440.2:p.Gly441del
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.1156_1158delGGT
  hgvsp: ENSP00000375998.1:p.Gly386del
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3287_255+3289delGGT
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12929
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6934
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2650
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3081
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly386del
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: GACC
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD

19-37643489-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643489
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643489
    reference: chr 19
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1708C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3278C>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.1147C>T
  hgvsp: ENSP00000292841.5:p.His383Tyr
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1312C>T
  hgvsp: ENSP00000349440.2:p.His438Tyr
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+209C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.1147C>T
  hgvsp: ENSP00000375998.1:p.His383Tyr
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3278C>T
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5688
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38101
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12927
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1967
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6937
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
hgvs: p.His383Tyr
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

19-37643494-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643494
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643494
    reference: chr 19
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+204A>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.1142A>C
  hgvsp: ENSP00000292841.5:p.Lys381Thr
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3273A>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1713A>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3273A>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1307A>C
  hgvsp: ENSP00000349440.2:p.Lys436Thr
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.1142A>C
  hgvsp: ENSP00000375998.1:p.Lys381Thr
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12933
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38084
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5694
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1967
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3083
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2765
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Lys381Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

19-37643522-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643522
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643522
    reference: chr 19
allele count: 6886
allele frequency: 5.672438506021715e-2
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.1114G>A
  hgvsp: ENSP00000375998.1:p.Ala372Thr
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1741G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3245G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3245G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+176G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1279G>A
  hgvsp: ENSP00000349440.2:p.Ala427Thr
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.1114G>A
  hgvsp: ENSP00000292841.5:p.Ala372Thr
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 178
genotype depth: GenotypeDepth
  all individuals: 5097
  bin: 3.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 106
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 133
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 3.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 34117
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 11609
  bin: 2.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.75e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.25e1
  variant carriers: 173
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.75e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 5958
  bin: 9.75e1
  variant carriers: 5231
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.25e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.25e1
  variant carriers: 197
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6139
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2331
  bin: 7.25e1
  variant carriers: 2
hgvs: p.Ala372Thr
num of homozygotes: 339
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/19-37643535-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643535
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643535
    reference: chr 19
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1266G>T
  hgvsp: ENSP00000349440.2:p.Lys422Asn
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1754G>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+163G>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3232G>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.1101G>T
  hgvsp: ENSP00000375998.1:p.Lys367Asn
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.1101G>T
  hgvsp: ENSP00000292841.5:p.Lys367Asn
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3232G>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5252
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11812
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8234
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1812
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys367Asn
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

19-37643539-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643539
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643539
    reference: chr 19
allele count: 2
allele frequency: 1.647555028337947e-5
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1758A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3228A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.1097A>G
  hgvsp: ENSP00000375998.1:p.Gln366Arg
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1262A>G
  hgvsp: ENSP00000349440.2:p.Gln421Arg
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.1097A>G
  hgvsp: ENSP00000292841.5:p.Gln366Arg
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+159A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3228A>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5252
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2592
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2378
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8236
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 6241
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln366Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

19-37643541-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643541
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643541
    reference: chr 19
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.1095T>C
  hgvsp: ENST00000392157.2:c.1095T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1260T>C
  hgvsp: ENST00000356958.4:c.1260T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.1095T>C
  hgvsp: ENST00000292841.5:c.1095T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3226T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+157T>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1760T>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3226T>C
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5252
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11809
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2591
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37788
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2377
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ile365Ile
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

19-37643547-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643547
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643547
    reference: chr 19
allele count: 48
allele frequency: 3.954262365307938e-4
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+151C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3220C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1766C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.1089C>T
  hgvsp: ENST00000292841.5:c.1089C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.1089C>T
  hgvsp: ENST00000392157.2:c.1089C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1254C>T
  hgvsp: ENST00000356958.4:c.1254C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3220C>T
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 34098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5245
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 9.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11803
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2376
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6235
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8269
  bin: 9.75e1
  variant carriers: 48
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala363Ala
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ

19-37643568-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643568
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643568
    reference: chr 19
allele count: 1101
allele frequency: 9.070388189547222e-3
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3199A>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1787A>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.1068A>C
  hgvsp: ENST00000392157.2:c.1068A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3199A>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1233A>C
  hgvsp: ENST00000356958.4:c.1233A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.1068A>C
  hgvsp: ENST00000292841.5:c.1068A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+130A>C
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 8.75e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 9.25e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 8.25e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 7.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 5159
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 6.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33357
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 4.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11590
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 3182
  bin: 9.75e1
  variant carriers: 636
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 3.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 36817
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1775
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2786
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile356Ile
num of homozygotes: 10
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

19-37643572-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643572
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643572
    reference: chr 19
allele count: 2
allele frequency: 1.647717910693689e-5
allele num: 121380
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.1064A>G
  hgvsp: ENSP00000375998.1:p.Tyr355Cys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3195A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.1064A>G
  hgvsp: ENSP00000292841.5:p.Tyr355Cys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1791A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1229A>G
  hgvsp: ENSP00000349440.2:p.Tyr410Cys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+126A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3195A>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5164
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6079
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Tyr355Cys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

19-37643574-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643574
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643574
    reference: chr 19
allele count: 5
allele frequency: 4.119905736556747e-5
allele num: 121362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3193G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.1062G>A
  hgvsp: ENST00000392157.2:c.1062G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.1062G>A
  hgvsp: ENST00000292841.5:c.1062G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3193G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1793G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+124G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1227G>A
  hgvsp: ENST00000356958.4:c.1227G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33324
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5179
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11608
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2327
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36761
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2790
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1777
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser354Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

19-37643575-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643575
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643575
    reference: chr 19
allele count: 5
allele frequency: 4.119702063146793e-5
allele num: 121368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+123C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1226C>T
  hgvsp: ENSP00000349440.2:p.Ser409Leu
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3192C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3192C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.1061C>T
  hgvsp: ENSP00000375998.1:p.Ser354Leu
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.1061C>T
  hgvsp: ENSP00000292841.5:p.Ser354Leu
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1794C>T
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5165
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2326
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9145
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser354Leu
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD

19-37643583-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643583
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643583
    reference: chr 19
allele count: 2
allele frequency: 1.647826516824309e-5
allele num: 121372
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1802A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1218A>G
  hgvsp: ENST00000356958.4:c.1218A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.1053A>G
  hgvsp: ENST00000292841.5:c.1053A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3184A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.1053A>G
  hgvsp: ENST00000392157.2:c.1053A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3184A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+115A>G
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5157
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6082
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2790
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9145
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly351Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP

19-37643589-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643589
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643589
    reference: chr 19
allele count: 2
allele frequency: 1.647799363949445e-5
allele num: 121374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+109T>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.1047T>C
  hgvsp: ENST00000392157.2:c.1047T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3178T>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1212T>C
  hgvsp: ENST00000356958.4:c.1212T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.1047T>C
  hgvsp: ENST00000292841.5:c.1047T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3178T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1808T>C
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11669
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2889
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33284
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5171
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2790
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36851
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2328
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
hgvs: p.His349His
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP

19-37643604-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643604
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643604
    reference: chr 19
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+94G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3163G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1823G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.1032G>A
  hgvsp: ENST00000392157.2:c.1032G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3163G>A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.1032G>A
  hgvsp: ENST00000292841.5:c.1032G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1197G>A
  hgvsp: ENST00000356958.4:c.1197G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11745
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33271
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2790
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6097
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val344Val
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: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

19-37643623-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643623
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643623
    reference: chr 19
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3144A>G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.1013A>G
  hgvsp: ENSP00000292841.5:p.Gln338Arg
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1178A>G
  hgvsp: ENSP00000349440.2:p.Gln393Arg
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1842A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3144A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.1013A>G
  hgvsp: ENSP00000375998.1:p.Gln338Arg
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+75A>G
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5206
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11795
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33292
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37134
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9149
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1782
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gln338Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD

19-37643632-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643632
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643632
    reference: chr 19
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.1004C>T
  hgvsp: ENSP00000292841.5:p.Ala335Val
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1169C>T
  hgvsp: ENSP00000349440.2:p.Ala390Val
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1851C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3135C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3135C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+66C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.1004C>T
  hgvsp: ENSP00000375998.1:p.Ala335Val
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33283
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5204
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2796
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1781
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6111
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala335Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

19-37643635-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643635
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643635
    reference: chr 19
allele count: 146
allele frequency: 1.202873714737675e-3
allele num: 121376
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1854A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+63A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3132A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1166A>G
  hgvsp: ENSP00000349440.2:p.Lys389Arg
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.1001A>G
  hgvsp: ENSP00000292841.5:p.Lys334Arg
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3132A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.1001A>G
  hgvsp: ENSP00000375998.1:p.Lys334Arg
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5190
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 3.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2925
  bin: 9.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 33216
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 11777
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6093
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2788
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9266
  bin: 9.75e1
  variant carriers: 135
hgvs: p.Lys334Arg
num of homozygotes: 2
population: Other
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

19-37643646-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643646
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643646
    reference: chr 19
allele count: 2
allele frequency: 1.64774506088418e-5
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1865T>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3121T>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.990T>C
  hgvsp: ENST00000392157.2:c.990T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.990T>C
  hgvsp: ENST00000292841.5:c.990T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+52T>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1155T>C
  hgvsp: ENST00000356958.4:c.1155T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3121T>C
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5195
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11790
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2333
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser330Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

19-37643656-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643656
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643656
    reference: chr 19
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3111A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3111A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1145A>G
  hgvsp: ENSP00000349440.2:p.Tyr382Cys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+42A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.980A>G
  hgvsp: ENSP00000292841.5:p.Tyr327Cys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.980A>G
  hgvsp: ENSP00000375998.1:p.Tyr327Cys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1875A>G
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33132
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5201
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11783
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2795
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36991
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1774
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Tyr327Cys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ

19-37643663-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643663
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643663
    reference: chr 19
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3104A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+35A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1138A>G
  hgvsp: ENSP00000349440.2:p.Lys380Glu
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1882A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.973A>G
  hgvsp: ENSP00000375998.1:p.Lys325Glu
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.973A>G
  hgvsp: ENSP00000292841.5:p.Lys325Glu
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3104A>G
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33095
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11754
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5198
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1775
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2790
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36927
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Lys325Glu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/19-37643680-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643680
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643680
    reference: chr 19
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+18G>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.956G>T
  hgvsp: ENSP00000375998.1:p.Arg319Ile
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1121G>T
  hgvsp: ENSP00000349440.2:p.Arg374Ile
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.956G>T
  hgvsp: ENSP00000292841.5:p.Arg319Ile
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3087G>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3087G>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1899G>T
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 11541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36246
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg319Ile
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

19-37643690-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643690
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643690
    reference: chr 19
allele count: 1
allele frequency: 8.244023083264634e-6
allele num: 121300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3077A>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1111A>T
  hgvsp: ENSP00000349440.2:p.Ile371Phe
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.946A>T
  hgvsp: ENSP00000292841.5:p.Ile316Phe
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.946A>T
  hgvsp: ENSP00000375998.1:p.Ile316Phe
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1909A>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+8A>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3077A>T
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11398
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35472
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5993
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 636
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1774
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile316Phe
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP

19-37643696-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643696
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643696
    reference: chr 19
allele count: 225
allele frequency: 1.855088714464745e-3
allele num: 121288
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.940T>A
  hgvsp: ENSP00000375998.1:p.Leu314Met
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3071T>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.940T>A
  hgvsp: ENSP00000292841.5:p.Leu314Met
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1105T>A
  hgvsp: ENSP00000349440.2:p.Leu369Met
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.938+2T>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1915T>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3071T>A
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5098
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 8.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 32512
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 9.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 6.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 11421
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 7.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 9.75e1
  variant carriers: 93
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 8.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1767
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35398
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 4.75e1
  variant carriers: 0
hgvs: c.938+2T>A
num of homozygotes: 2
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD

19-37643701-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643701
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643701
    reference: chr 19
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1920C>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3066C>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.935C>G
  hgvsp: ENSP00000375998.1:p.Ser312Ter
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1100C>G
  hgvsp: ENSP00000349440.2:p.Ser367Ter
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.935C>G
  hgvsp: ENSP00000292841.5:p.Ser312Ter
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.935C>G
  hgvsp: ENSP00000347724.2:p.Ser312Ter
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3066C>G
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2993
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9407
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser312Ter
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ

19-37643707-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643707
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643707
    reference: chr 19
allele count: 2
allele frequency: 1.648695881557688e-5
allele num: 121308
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1094A>G
  hgvsp: ENSP00000349440.2:p.Tyr365Cys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3060A>G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.929A>G
  hgvsp: ENSP00000292841.5:p.Tyr310Cys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.929A>G
  hgvsp: ENSP00000375998.1:p.Tyr310Cys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.929A>G
  hgvsp: ENSP00000347724.2:p.Tyr310Cys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1926A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3060A>G
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32550
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5111
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2804
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9411
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2323
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Tyr310Cys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD

19-37643709-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643709
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643709
    reference: chr 19
allele count: 2
allele frequency: 1.648886177387175e-5
allele num: 121294
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.927C>T
  hgvsp: ENST00000392157.2:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3058C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.927C>T
  hgvsp: ENST00000355533.2:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.927C>T
  hgvsp: ENST00000292841.5:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1928C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3058C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1092C>T
  hgvsp: ENST00000356958.4:c.1092C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11530
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32604
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2996
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35842
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr309Thr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP

19-37643717-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643717
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643717
    reference: chr 19
allele count: 7
allele frequency: 5.77062586559388e-5
allele num: 121304
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1084G>C
  hgvsp: ENSP00000349440.2:p.Ala362Pro
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.919G>C
  hgvsp: ENSP00000292841.5:p.Ala307Pro
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.919G>C
  hgvsp: ENSP00000375998.1:p.Ala307Pro
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3050G>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.919G>C
  hgvsp: ENSP00000347724.2:p.Ala307Pro
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1936G>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3050G>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11646
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2998
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6110
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1806
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2830
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala307Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

19-37643721-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643721
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643721
    reference: chr 19
allele count: 20
allele frequency: 1.648559982854976e-4
allele num: 121318
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3046G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1940G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3046G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1080G>A
  hgvsp: ENST00000356958.4:c.1080G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.915G>A
  hgvsp: ENST00000392157.2:c.915G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.915G>A
  hgvsp: ENST00000292841.5:c.915G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.915G>A
  hgvsp: ENST00000355533.2:c.915G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32749
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11705
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 675
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly305Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD

19-37643731-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643731
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643731
    reference: chr 19
allele count: 2
allele frequency: 1.648261084555794e-5
allele num: 121340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.905C>T
  hgvsp: ENSP00000347724.2:p.Thr302Ile
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1070C>T
  hgvsp: ENSP00000349440.2:p.Thr357Ile
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1950C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3036C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.905C>T
  hgvsp: ENSP00000375998.1:p.Thr302Ile
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.905C>T
  hgvsp: ENSP00000292841.5:p.Thr302Ile
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3036C>T
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32776
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11824
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36358
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2390
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr302Ile
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: G
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-37643738-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643738
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643738
    reference: chr 19
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3029A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3029A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1063A>G
  hgvsp: ENSP00000349440.2:p.Ile355Val
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1957A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.898A>G
  hgvsp: ENSP00000347724.2:p.Ile300Val
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.898A>G
  hgvsp: ENSP00000292841.5:p.Ile300Val
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.898A>G
  hgvsp: ENSP00000375998.1:p.Ile300Val
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11864
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5274
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3012
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2906
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2398
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6204
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36434
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ile300Val
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

19-37643740-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643740
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643740
    reference: chr 19
allele count: 2
allele frequency: 1.647826516824309e-5
allele num: 121372
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.896C>G
  hgvsp: ENSP00000347724.2:p.Ser299Cys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3027C>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1959C>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3027C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1061C>G
  hgvsp: ENSP00000349440.2:p.Ser354Cys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.896C>G
  hgvsp: ENSP00000375998.1:p.Ser299Cys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.896C>G
  hgvsp: ENSP00000292841.5:p.Ser299Cys
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 32813
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11865
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3012
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5278
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2397
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1861
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser299Cys
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-37643743-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643743
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643743
    reference: chr 19
allele count: 3
allele frequency: 2.47161759132627e-5
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.893C>T
  hgvsp: ENSP00000292841.5:p.Ser298Phe
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3024C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3024C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1058C>T
  hgvsp: ENSP00000349440.2:p.Ser353Phe
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1962C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.893C>T
  hgvsp: ENSP00000375998.1:p.Ser298Phe
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.893C>T
  hgvsp: ENSP00000347724.2:p.Ser298Phe
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5287
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 32819
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9462
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2399
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 690
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser298Phe
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

19-37643750-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643750
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643750
    reference: chr 19
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.886G>A
  hgvsp: ENSP00000375998.1:p.Glu296Lys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3017G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1969G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3017G>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.886G>A
  hgvsp: ENSP00000292841.5:p.Glu296Lys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.886G>A
  hgvsp: ENSP00000347724.2:p.Glu296Lys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1051G>A
  hgvsp: ENSP00000349440.2:p.Glu351Lys
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3015
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32819
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5291
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2403
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9465
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2913
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu296Lys
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD

19-37643754-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643754
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643754
    reference: chr 19
allele count: 8
allele frequency: 6.59043727551323e-5
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3013T>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.882T>C
  hgvsp: ENST00000392157.2:c.882T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.882T>C
  hgvsp: ENST00000292841.5:c.882T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1973T>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1047T>C
  hgvsp: ENST00000356958.4:c.1047T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.882T>C
  hgvsp: ENST00000355533.2:c.882T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3013T>C
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32818
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9464
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36459
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser294Ser
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

19-37643762-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643762
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643762
    reference: chr 19
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1981G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.874G>A
  hgvsp: ENSP00000347724.2:p.Val292Ile
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.874G>A
  hgvsp: ENSP00000375998.1:p.Val292Ile
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.874G>A
  hgvsp: ENSP00000292841.5:p.Val292Ile
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1039G>A
  hgvsp: ENSP00000349440.2:p.Val347Ile
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3005G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3005G>A
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11886
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1867
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val292Ile
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

19-37643764-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643764
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643764
    reference: chr 19
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.872A>C
  hgvsp: ENSP00000292841.5:p.Lys291Thr
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3003A>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1983A>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.872A>C
  hgvsp: ENSP00000347724.2:p.Lys291Thr
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1037A>C
  hgvsp: ENSP00000349440.2:p.Lys346Thr
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3003A>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.872A>C
  hgvsp: ENSP00000375998.1:p.Lys291Thr
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32815
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5297
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11885
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36472
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1868
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2404
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Lys291Thr
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD

19-37643765-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643765
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643765
    reference: chr 19
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1036A>G
  hgvsp: ENSP00000349440.2:p.Lys346Glu
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.871A>G
  hgvsp: ENSP00000375998.1:p.Lys291Glu
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.871A>G
  hgvsp: ENSP00000292841.5:p.Lys291Glu
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+3002A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.871A>G
  hgvsp: ENSP00000347724.2:p.Lys291Glu
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+3002A>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1984A>G
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32814
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11886
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5297
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2404
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9469
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Lys291Glu
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD

19-37643772-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643772
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643772
    reference: chr 19
allele count: 55
allele frequency: 4.530403123507026e-4
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.864A>C
  hgvsp: ENST00000292841.5:c.864A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1029A>C
  hgvsp: ENST00000356958.4:c.1029A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2995A>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.864A>C
  hgvsp: ENST00000392157.2:c.864A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.864A>C
  hgvsp: ENST00000355533.2:c.864A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1991A>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2995A>C
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5298
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11872
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32796
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3055
  bin: 9.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36451
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1866
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr288Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

19-37643777-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643777
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643777
    reference: chr 19
allele count: 7720
allele frequency: 6.358933807782281e-2
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1996G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.859G>A
  hgvsp: ENSP00000375998.1:p.Val287Ile
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.859G>A
  hgvsp: ENSP00000292841.5:p.Val287Ile
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1024G>A
  hgvsp: ENSP00000349440.2:p.Val342Ile
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.859G>A
  hgvsp: ENSP00000347724.2:p.Val287Ile
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2990G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2990G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.75e1
  variant carriers: 115
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7442
  bin: 9.75e1
  variant carriers: 6286
genotype depth: GenotypeDepth
  all individuals: 11571
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 9.25e1
  variant carriers: 159
genotype depth: GenotypeDepth
  all individuals: 32308
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.25e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 115
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.25e1
  variant carriers: 129
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1773
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2321
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val287Ile
num of homozygotes: 521
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

19-37643778-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643778
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643778
    reference: chr 19
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.858C>T
  hgvsp: ENST00000392157.2:c.858C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.858C>T
  hgvsp: ENST00000355533.2:c.858C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-1997C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2989C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2989C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.858C>T
  hgvsp: ENST00000292841.5:c.858C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1023C>T
  hgvsp: ENST00000356958.4:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11597
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6946
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32312
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6062
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2331
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu286Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

19-37643781-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643781
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643781
    reference: chr 19
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1020C>T
  hgvsp: ENST00000356958.4:c.1020C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.855C>T
  hgvsp: ENST00000392157.2:c.855C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2000C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.855C>T
  hgvsp: ENST00000355533.2:c.855C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.855C>T
  hgvsp: ENST00000292841.5:c.855C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2986C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2986C>T
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5126
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6946
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32311
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6060
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2331
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asn285Asn
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/19-37643797-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643797
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643797
    reference: chr 19
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.839T>G
  hgvsp: ENSP00000292841.5:p.Phe280Cys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.1004T>G
  hgvsp: ENSP00000349440.2:p.Phe335Cys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2970T>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.839T>G
  hgvsp: ENSP00000347724.2:p.Phe280Cys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2970T>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.839T>G
  hgvsp: ENSP00000375998.1:p.Phe280Cys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2016T>G
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6946
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10556
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2330
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35858
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Phe280Cys
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-37643806-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643806
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643806
    reference: chr 19
allele count: 2
allele frequency: 1.647310765175851e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.995G>A
  hgvsp: ENSP00000349440.2:p.Gly332Glu
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.830G>A
  hgvsp: ENSP00000292841.5:p.Gly277Glu
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2961G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2025G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.830G>A
  hgvsp: ENSP00000347724.2:p.Gly277Glu
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2961G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.830G>A
  hgvsp: ENSP00000375998.1:p.Gly277Glu
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6947
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5126
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1793
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2330
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6060
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10557
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly277Glu
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

19-37643808-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643808
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643808
    reference: chr 19
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2959T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2027T>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2959T>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.828T>C
  hgvsp: ENST00000392157.2:c.828T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.828T>C
  hgvsp: ENST00000292841.5:c.828T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.828T>C
  hgvsp: ENST00000355533.2:c.828T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.993T>C
  hgvsp: ENST00000356958.4:c.993T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6948
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32308
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2330
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35861
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1794
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Tyr276Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

19-37643813-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643813
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643813
    reference: chr 19
allele count: 2
allele frequency: 1.647310765175851e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2954G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.823G>A
  hgvsp: ENSP00000347724.2:p.Glu275Lys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2954G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2032G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.823G>A
  hgvsp: ENSP00000292841.5:p.Glu275Lys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.988G>A
  hgvsp: ENSP00000349440.2:p.Glu330Lys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.823G>A
  hgvsp: ENSP00000375998.1:p.Glu275Lys
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5126
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6949
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11600
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1793
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2330
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu275Lys
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

19-37643814-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643814
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643814
    reference: chr 19
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2953C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.822C>T
  hgvsp: ENST00000355533.2:c.822C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2033C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.822C>T
  hgvsp: ENST00000392157.2:c.822C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2953C>T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.822C>T
  hgvsp: ENST00000292841.5:c.822C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.987C>T
  hgvsp: ENST00000356958.4:c.987C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32308
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6948
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr274Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

19-37643815-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643815
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643815
    reference: chr 19
allele count: 4
allele frequency: 3.294621530351701e-5
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.986C>T
  hgvsp: ENSP00000349440.2:p.Thr329Ile
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2034C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.821C>T
  hgvsp: ENSP00000347724.2:p.Thr274Ile
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2952C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2952C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.821C>T
  hgvsp: ENSP00000292841.5:p.Thr274Ile
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.821C>T
  hgvsp: ENSP00000375998.1:p.Thr274Ile
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6951
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32305
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2826
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr274Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

19-37643822-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643822
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643822
    reference: chr 19
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.814A>G
  hgvsp: ENSP00000375998.1:p.Ile272Val
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2945A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2945A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.979A>G
  hgvsp: ENSP00000349440.2:p.Ile327Val
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2041A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.814A>G
  hgvsp: ENSP00000347724.2:p.Ile272Val
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.814A>G
  hgvsp: ENSP00000292841.5:p.Ile272Val
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 32304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6948
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35854
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10563
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile272Val
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

19-37643823-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643823
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643823
    reference: chr 19
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.813T>C
  hgvsp: ENST00000292841.5:c.813T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2944T>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.813T>C
  hgvsp: ENST00000355533.2:c.813T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2042T>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.813T>C
  hgvsp: ENST00000392157.2:c.813T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.978T>C
  hgvsp: ENST00000356958.4:c.978T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2944T>C
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6948
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2330
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6059
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Tyr271Tyr
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum

19-37643828-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643828
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643828
    reference: chr 19
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.973C>T
  hgvsp: ENSP00000349440.2:p.Pro325Ser
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2047C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.808C>T
  hgvsp: ENSP00000375998.1:p.Pro270Ser
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2939C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.808C>T
  hgvsp: ENSP00000292841.5:p.Pro270Ser
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2939C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.808C>T
  hgvsp: ENSP00000347724.2:p.Pro270Ser
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6949
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32305
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1794
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35856
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro270Ser
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

19-37643834-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643834
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643834
    reference: chr 19
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.802G>C
  hgvsp: ENSP00000375998.1:p.Val268Leu
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2053G>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.967G>C
  hgvsp: ENSP00000349440.2:p.Val323Leu
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.802G>C
  hgvsp: ENSP00000292841.5:p.Val268Leu
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2933G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2933G>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.802G>C
  hgvsp: ENSP00000347724.2:p.Val268Leu
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6949
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2827
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1794
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2330
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val268Leu
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

19-37643835-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643835
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643835
    reference: chr 19
allele count: 4
allele frequency: 3.294567258590584e-5
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.801A>G
  hgvsp: ENST00000292841.5:c.801A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2054A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.801A>G
  hgvsp: ENST00000355533.2:c.801A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.801A>G
  hgvsp: ENST00000392157.2:c.801A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.966A>G
  hgvsp: ENST00000356958.4:c.966A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2932A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2932A>G
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6951
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2330
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2827
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1794
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg267Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

19-37643838-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643838
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643838
    reference: chr 19
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.798A>G
  hgvsp: ENST00000292841.5:c.798A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.798A>G
  hgvsp: ENST00000355533.2:c.798A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.963A>G
  hgvsp: ENST00000356958.4:c.963A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.798A>G
  hgvsp: ENST00000392157.2:c.798A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2929A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2929A>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2057A>G
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6950
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2827
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr266Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

19-37643840-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643840
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643840
    reference: chr 19
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.796A>G
  hgvsp: ENSP00000292841.5:p.Thr266Ala
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2927A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2927A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.796A>G
  hgvsp: ENSP00000375998.1:p.Thr266Ala
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2059A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.796A>G
  hgvsp: ENSP00000347724.2:p.Thr266Ala
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.961A>G
  hgvsp: ENSP00000349440.2:p.Thr321Ala
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6951
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6059
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10568
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr266Ala
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD

19-37643843-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643843
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643843
    reference: chr 19
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.793C>A
  hgvsp: ENSP00000347724.2:p.His265Asn
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2924C>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.793C>A
  hgvsp: ENSP00000292841.5:p.His265Asn
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.793C>A
  hgvsp: ENSP00000375998.1:p.His265Asn
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.958C>A
  hgvsp: ENSP00000349440.2:p.His320Asn
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2924C>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2062C>A
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32300
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6951
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10569
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35853
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
hgvs: p.His265Asn
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

19-37643848-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643848
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643848
    reference: chr 19
allele count: 7
allele frequency: 5.765492702533522e-5
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.788G>A
  hgvsp: ENSP00000347724.2:p.Arg263His
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2067G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.788G>A
  hgvsp: ENSP00000292841.5:p.Arg263His
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.788G>A
  hgvsp: ENSP00000375998.1:p.Arg263His
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2919G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2919G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.953G>A
  hgvsp: ENSP00000349440.2:p.Arg318His
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6956
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2826
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2330
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg263His
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

19-37643849-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643849
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643849
    reference: chr 19
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2918C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.787C>T
  hgvsp: ENSP00000347724.2:p.Arg263Cys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2918C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.787C>T
  hgvsp: ENSP00000375998.1:p.Arg263Cys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.787C>T
  hgvsp: ENSP00000292841.5:p.Arg263Cys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2068C>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.952C>T
  hgvsp: ENSP00000349440.2:p.Arg318Cys
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6953
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11597
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35849
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2826
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg263Cys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
reference allele: G
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

19-37643861-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643861
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643861
    reference: chr 19
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.775C>G
  hgvsp: ENSP00000347724.2:p.Gln259Glu
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  clinical significance: not_provided
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2906C>G
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2906C>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.940C>G
  hgvsp: ENSP00000349440.2:p.Gln314Glu
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2080C>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.775C>G
  hgvsp: ENSP00000375998.1:p.Gln259Glu
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.775C>G
  hgvsp: ENSP00000292841.5:p.Gln259Glu
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6954
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gln259Glu
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-37643865-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643865
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643865
    reference: chr 19
allele count: 2
allele frequency: 1.647283629295292e-5
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.771A>G
  hgvsp: ENST00000355533.2:c.771A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.936A>G
  hgvsp: ENST00000356958.4:c.936A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2084A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.771A>G
  hgvsp: ENST00000292841.5:c.771A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2902A>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.771A>G
  hgvsp: ENST00000392157.2:c.771A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2902A>G
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6955
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2826
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2330
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35845
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10577
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Gln257Gln
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD

19-37643871-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643871
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643871
    reference: chr 19
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2896G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2896G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.765G>A
  hgvsp: ENST00000355533.2:c.765G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.765G>A
  hgvsp: ENST00000392157.2:c.765G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2090G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.930G>A
  hgvsp: ENST00000356958.4:c.930G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.765G>A
  hgvsp: ENST00000292841.5:c.765G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6956
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10578
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6057
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2826
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Lys255Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

19-37643884-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643884
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643884
    reference: chr 19
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.752C>G
  hgvsp: ENSP00000292841.5:p.Ser251Cys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2103C>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.917C>G
  hgvsp: ENSP00000349440.2:p.Ser306Cys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2883C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2883C>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.752C>G
  hgvsp: ENSP00000347724.2:p.Ser251Cys
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.752C>G
  hgvsp: ENSP00000375998.1:p.Ser251Cys
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 11593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32293
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6957
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2826
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10579
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser251Cys
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ

19-37643892-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643892
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643892
    reference: chr 19
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2875T>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.744T>C
  hgvsp: ENST00000392157.2:c.744T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.909T>C
  hgvsp: ENST00000356958.4:c.909T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.744T>C
  hgvsp: ENST00000355533.2:c.744T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2111T>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.744T>C
  hgvsp: ENST00000292841.5:c.744T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2875T>C
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6957
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2329
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1795
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Cys248Cys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

19-37643899-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643899
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643899
    reference: chr 19
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2868G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.902G>A
  hgvsp: ENSP00000349440.2:p.Ser301Asn
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2868G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2118G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.737G>A
  hgvsp: ENSP00000375998.1:p.Ser246Asn
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.737G>A
  hgvsp: ENSP00000347724.2:p.Ser246Asn
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.737G>A
  hgvsp: ENSP00000292841.5:p.Ser246Asn
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6957
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6057
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1795
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser246Asn
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

19-37643904-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643904
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643904
    reference: chr 19
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2123G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.732G>A
  hgvsp: ENST00000392157.2:c.732G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2863G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2863G>A
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.732G>A
  hgvsp: ENST00000355533.2:c.732G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.732G>A
  hgvsp: ENST00000292841.5:c.732G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.897G>A
  hgvsp: ENST00000356958.4:c.897G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6957
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35832
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1795
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu244Glu
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

19-37643915-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643915
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643915
    reference: chr 19
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2852A>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.721A>T
  hgvsp: ENSP00000292841.5:p.Lys241Ter
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.721A>T
  hgvsp: ENSP00000375998.1:p.Lys241Ter
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2134A>T
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.886A>T
  hgvsp: ENSP00000349440.2:p.Lys296Ter
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2852A>T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.721A>T
  hgvsp: ENSP00000347724.2:p.Lys241Ter
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6958
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35831
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10581
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2329
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2826
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Lys241Ter
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD

19-37643923-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643923
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643923
    reference: chr 19
allele count: 8
allele frequency: 6.589134517181169e-5
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.878C>G
  hgvsp: ENSP00000349440.2:p.Thr293Ser
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.713C>G
  hgvsp: ENSP00000347724.2:p.Thr238Ser
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2844C>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.713C>G
  hgvsp: ENSP00000292841.5:p.Thr238Ser
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2844C>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2142C>G
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.713C>G
  hgvsp: ENSP00000375998.1:p.Thr238Ser
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32269
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6961
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2826
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6056
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr238Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-37643925-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 37643925
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 37643925
    reference: chr 19
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000349440
  ensembl transcript: ENST00000356958
  gene symbol: ZNF585A
  hgvsc: ENST00000356958.4:c.876T>C
  hgvsp: ENST00000356958.4:c.876T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000347724
  ensembl transcript: ENST00000355533
  gene symbol: ZNF585A
  hgvsc: ENST00000355533.2:c.711T>C
  hgvsp: ENST00000355533.2:c.711T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl transcript: ENST00000588723
  gene symbol: ZNF585A
  hgvsc: ENST00000588723.1:n.502+2842T>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000375998
  ensembl transcript: ENST00000392157
  gene symbol: ZNF585A
  hgvsc: ENST00000392157.2:c.711T>C
  hgvsp: ENST00000392157.2:c.711T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000267360
  ensembl protein: ENSP00000465212
  ensembl transcript: ENST00000588873
  gene symbol: CTC-454I21.3
  hgvsc: ENST00000588873.1:c.255+2842T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000466825
  ensembl transcript: ENST00000587817
  gene symbol: ZNF585A
  hgvsc: ENST00000587817.1:c.293-2144T>C
  variant of: http://identifiers.org/hgnc/26305
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196967
  ensembl protein: ENSP00000292841
  ensembl transcript: ENST00000292841
  gene symbol: ZNF585A
  hgvsc: ENST00000292841.5:c.711T>C
  hgvsp: ENST00000292841.5:c.711T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26305
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32269
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6960
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.75e1
  variant carriers: 0
hgvs: p.His237His
num of homozygotes: 0
reference allele: A

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

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 721
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2647
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2758
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.42e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.324e0

FS
type: SiteQuality
SIO_000300: 2.515e0

DP
type: SiteQuality
SIO_000300: 1.636495e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.7e-1

MQ
type: SiteQuality
SIO_000300: 5.356e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.02e-1

QD
type: SiteQuality
SIO_000300: 1.132e1

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2758
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 721
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3080
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -3.681e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.64e0

MQRankSum
type: SiteQuality
SIO_000300: 2.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.72e0

MQ
type: SiteQuality
SIO_000300: 5.474e1

QD
type: SiteQuality
SIO_000300: 1.324e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.79e-2

FS
type: SiteQuality
SIO_000300: 4.064e0

DP
type: SiteQuality
SIO_000300: 1.636541e6

GenotypeQuality
all individuals: 1967
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 672
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2759
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3080
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2648
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.071e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.06e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.77e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.032e0

MQRankSum
type: SiteQuality
SIO_000300: 9.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.28e1

FS
type: SiteQuality
SIO_000300: 2.75e0

DP
type: SiteQuality
SIO_000300: 1.636592e6

MQ
type: SiteQuality
SIO_000300: 5.306e1

GenotypeQuality
all individuals: 6936
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41821
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 721
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1967
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 9.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.175e1

QD
type: SiteQuality
SIO_000300: 1.323e1

DP
type: SiteQuality
SIO_000300: 1.636624e6

MQRankSum
type: SiteQuality
SIO_000300: 1.46e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.51e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.571e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.52e-1

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

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2764
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 721
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1967
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41832
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
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: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.491983577571999e-5
allele num: 66738
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

MQ
type: SiteQuality
SIO_000300: 5.389e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -9.67e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.127e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.91e-1

DP
type: SiteQuality
SIO_000300: 1.63697e6

FS
type: SiteQuality
SIO_000300: 4.362e0

QD
type: SiteQuality
SIO_000300: 1.129e1

VQSLOD
type: SiteQuality
SIO_000300: 1.49e0

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

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

GenotypeQuality
all individuals: 2649
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3082
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2764
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 721
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41815
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 1.177e0

QD
type: SiteQuality
SIO_000300: 7.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.64e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.93e0

MQRankSum
type: SiteQuality
SIO_000300: -5.141e0

MQ
type: SiteQuality
SIO_000300: 5.113e1

VQSLOD
type: SiteQuality
SIO_000300: -4.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.636897e6

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2650
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6938
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41794
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 671
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
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: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.56e-1

QD
type: SiteQuality
SIO_000300: 1.37e1

MQ
type: SiteQuality
SIO_000300: 5.616e1

DP
type: SiteQuality
SIO_000300: 1.637039e6

VQSLOD
type: SiteQuality
SIO_000300: -1.339e0

FS
type: SiteQuality
SIO_000300: 1.744e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.7e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.03e0

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

GenotypeQuality
all individuals: 8856
bin: 9.75e1
variant carriers: 6537

GenotypeQuality
all individuals: 37548
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1757
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2780
bin: 7.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 395
allele frequency: 5.972180223767765e-2
allele num: 6614
num of homozygotes: 12

Other
type: Population
allele count: 60
allele frequency: 6.607929515418502e-2
allele num: 908
num of homozygotes: 2

South Asian
type: Population
allele count: 420
allele frequency: 2.543912780133253e-2
allele num: 16510
num of homozygotes: 10

African
type: Population
allele count: 2055
allele frequency: 1.976721816083109e-1
allele num: 10396
num of homozygotes: 203

European (Non-Finnish)
type: Population
allele count: 2208
allele frequency: 3.308559098537521e-2
allele num: 66736
num of homozygotes: 40

Latino
type: Population
allele count: 985
allele frequency: 8.50898410504492e-2
allele num: 11576
num of homozygotes: 41

East Asian
type: Population
allele count: 763
allele frequency: 8.816732146984053e-2
allele num: 8654
num of homozygotes: 31

MQ
type: SiteQuality
SIO_000300: 5.432e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.25e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.375e0

MQRankSum
type: SiteQuality
SIO_000300: -1.081e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.334e1

DP
type: SiteQuality
SIO_000300: 2.320485e6

VQSLOD
type: SiteQuality
SIO_000300: 1.31e0

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

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6243
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 673
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37795
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2379
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 635
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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: 8654
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.513e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.59e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.205e0

DP
type: SiteQuality
SIO_000300: 2.002706e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.09e0

MQRankSum
type: SiteQuality
SIO_000300: -2.939e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -7.829e0

QD
type: SiteQuality
SIO_000300: 1.361e1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
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 (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997242536866083e-5
allele num: 66728
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 6.42e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.492e0

VQSLOD
type: SiteQuality
SIO_000300: -2.572e0

MQ
type: SiteQuality
SIO_000300: 5.461e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.495e0

DP
type: SiteQuality
SIO_000300: 2.002737e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.59e0

QD
type: SiteQuality
SIO_000300: 1.254e1

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e0

MQ
type: SiteQuality
SIO_000300: 4.88e1

VQSLOD
type: SiteQuality
SIO_000300: -1.261e1

QD
type: SiteQuality
SIO_000300: 1.402e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -8.346e0

FS
type: SiteQuality
SIO_000300: 3.0698e1

DP
type: SiteQuality
SIO_000300: 2.002651e6

BaseQRankSum
type: SiteQuality
SIO_000300: 7.51e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.594e0

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

GenotypeQuality
all individuals: 36
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
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

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: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

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

African
type: Population
allele count: 46
allele frequency: 4.423076923076923e-3
allele num: 10400
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.73e-1

DP
type: SiteQuality
SIO_000300: 2.005706e6

VQSLOD
type: SiteQuality
SIO_000300: -8.399999999999999e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.74e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.352e0

QD
type: SiteQuality
SIO_000300: 1.502e1

MQ
type: SiteQuality
SIO_000300: 5.499e1

GenotypeQuality
all individuals: 6071
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2323
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variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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variant carriers: 1089

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 34
allele frequency: 2.936603903955778e-3
allele num: 11578
num of homozygotes: 0

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

South Asian
type: Population
allele count: 22
allele frequency: 1.332687181972377e-3
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 595
allele frequency: 8.917865707434053e-3
allele num: 66720
num of homozygotes: 2

Other
type: Population
allele count: 9
allele frequency: 9.911894273127754e-3
allele num: 908
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 149
allele frequency: 2.252797097066828e-2
allele num: 6614
num of homozygotes: 3

African
type: Population
allele count: 291
allele frequency: 2.797538934820227e-2
allele num: 10402
num of homozygotes: 5

QD
type: SiteQuality
SIO_000300: 1.503e1

VQSLOD
type: SiteQuality
SIO_000300: 3.2e-1

DP
type: SiteQuality
SIO_000300: 2.083787e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.74e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.12e-1

FS
type: SiteQuality
SIO_000300: 5.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.99e0

MQ
type: SiteQuality
SIO_000300: 5.236e1

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

GenotypeQuality
all individuals: 36857
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GenotypeQuality
all individuals: 69
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variant carriers: 0

GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 9136
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GenotypeQuality
all individuals: 2793
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GenotypeQuality
all individuals: 2330
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variant carriers: 0

GenotypeQuality
all individuals: 21
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GenotypeQuality
all individuals: 1778
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 9.25e1
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: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997691777331455e-5
allele num: 66718
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
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: 11578
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.16e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.06e-1

QD
type: SiteQuality
SIO_000300: 1.62e1

VQSLOD
type: SiteQuality
SIO_000300: -1.123e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

DP
type: SiteQuality
SIO_000300: 2.062142e6

FS
type: SiteQuality
SIO_000300: 4.551e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-1

MQ
type: SiteQuality
SIO_000300: 5.08e1

GenotypeQuality
all individuals: 629
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
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variant carriers: 0

GenotypeQuality
all individuals: 45
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 52
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GenotypeQuality
all individuals: 9141
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variant carriers: 5

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
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: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
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: 4
allele frequency: 5.99610253335332e-5
allele num: 66710
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

QD
type: SiteQuality
SIO_000300: 1.175e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

MQ
type: SiteQuality
SIO_000300: 5.096e1

FS
type: SiteQuality
SIO_000300: 7.73e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.403e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.35e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

DP
type: SiteQuality
SIO_000300: 2.062582e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.3e-2

GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.494229443328637e-5
allele num: 66718
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 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: 6612
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 9.91e-1

MQ
type: SiteQuality
SIO_000300: 5.277e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQRankSum
type: SiteQuality
SIO_000300: 5.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.445e0

DP
type: SiteQuality
SIO_000300: 2.062789e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

FS
type: SiteQuality
SIO_000300: 1.104e0

QD
type: SiteQuality
SIO_000300: 1.234e1

VQSLOD
type: SiteQuality
SIO_000300: -2.76e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 663
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

European (Finnish)
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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: 10400
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.15e0

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.86e-1

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.224e0

MQ
type: SiteQuality
SIO_000300: 5.214e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.062914e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 28
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GenotypeQuality
all individuals: 56
bin: 3.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997871511227029e-5
allele num: 66714
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

MQRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
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SIO_000300: 6.21e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.3e-1

FS
type: SiteQuality
SIO_000300: 1.978e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 4.933e1

QD
type: SiteQuality
SIO_000300: 1.414e1

DP
type: SiteQuality
SIO_000300: 2.063195e6

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

GenotypeQuality
all individuals: 2327
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GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 25
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GenotypeQuality
all individuals: 9150
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GenotypeQuality
all individuals: 2
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
allele num: 8654
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 6.058403004967891e-5
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num of homozygotes: 0

BaseQRankSum
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SIO_000300: -3.625e0

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.61e-1

MQ
type: SiteQuality
SIO_000300: 5.083e1

MQRankSum
type: SiteQuality
SIO_000300: 6.6e-2

DP
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -1.279e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

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

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

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

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

Latino
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allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

ReadPosRankSum
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SIO_000300: 1.02e0

BaseQRankSum
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SIO_000300: -2.76e-1

MQRankSum
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SIO_000300: -1.859e0

InbreedingCoeff
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SIO_000300: 1.31e-2

FS
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ClippingRankSum
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DP
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MQ
type: SiteQuality
SIO_000300: 4.612e1

VQSLOD
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SIO_000300: -1.876e0

QD
type: SiteQuality
SIO_000300: 1.195e1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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InbreedingCoeff
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MQ
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SIO_000300: 5.142e1

VQSLOD
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.590000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.19e0

MQRankSum
type: SiteQuality
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DP
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.362e0

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

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

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

South Asian
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allele count: 74
allele frequency: 4.482675066634359e-3
allele num: 16508
num of homozygotes: 2

Latino
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allele count: 9
allele frequency: 7.77336327517706e-4
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
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allele count: 56
allele frequency: 8.394291881520566e-4
allele num: 66712
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.91e-2

DP
type: SiteQuality
SIO_000300: 2.072885e6

QD
type: SiteQuality
SIO_000300: 7.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.42e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 9.021000000000001e0

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 4.427e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.67e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
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

DP
type: SiteQuality
SIO_000300: 2.069054e6

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.39e-1

MQ
type: SiteQuality
SIO_000300: 4.704e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.34e-1

FS
type: SiteQuality
SIO_000300: 2.684e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.6e-2

QD
type: SiteQuality
SIO_000300: 8.869999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-2

GenotypeQuality
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variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

Other
type: Population
allele count: 0
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.35e-1

VQSLOD
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.57e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.28e-2

BaseQRankSum
type: SiteQuality
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DP
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SIO_000300: 2.068413e6

FS
type: SiteQuality
SIO_000300: 1.907e0

MQRankSum
type: SiteQuality
SIO_000300: 5.96e-1

MQ
type: SiteQuality
SIO_000300: 4.696e1

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

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

South Asian
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allele frequency: 0.0e0
allele num: 16502
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Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499160470136723e-5
allele num: 66704
num of homozygotes: 0

East Asian
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Other
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African
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MQRankSum
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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DP
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InbreedingCoeff
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VQSLOD
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FS
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 4.067e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Other
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European (Non-Finnish)
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African
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East Asian
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allele num: 8654
num of homozygotes: 0

Latino
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MQ
type: SiteQuality
SIO_000300: 4.034e1

InbreedingCoeff
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QD
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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DP
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SIO_000300: 2.06311e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele num: 10380
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South Asian
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allele frequency: 6.067224851352991e-5
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Latino
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European (Finnish)
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allele num: 6614
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Other
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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QD
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VQSLOD
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FS
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MQRankSum
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MQ
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 1.511944360447536e-3
allele num: 6614
num of homozygotes: 0

East Asian
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South Asian
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allele frequency: 4.247572815533981e-4
allele num: 16480
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Latino
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allele frequency: 8.640055296353897e-5
allele num: 11574
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Other
type: Population
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allele num: 908
num of homozygotes: 0

African
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allele count: 5
allele frequency: 4.81881264456438e-4
allele num: 10376
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European (Non-Finnish)
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allele count: 201
allele frequency: 3.014306709456825e-3
allele num: 66682
num of homozygotes: 2

MQ
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SIO_000300: 4.087e1

BaseQRankSum
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VQSLOD
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DP
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MQRankSum
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ReadPosRankSum
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SIO_000300: 3.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.0e-2

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

QD
type: SiteQuality
SIO_000300: 1.294e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 241
bin: 3.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
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 (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499655079331754e-5
allele num: 66682
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

ReadPosRankSum
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QD
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DP
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 1.73e0

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

MQ
type: SiteQuality
SIO_000300: 5.046e1

GenotypeQuality
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variant carriers: 0

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

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

South Asian
type: Population
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allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 2.999220202747286e-5
allele num: 66684
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.362e1

VQSLOD
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.83e-1

MQRankSum
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DP
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SIO_000300: 2.077727e6

BaseQRankSum
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SIO_000300: 3.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.92e-1

FS
type: SiteQuality
SIO_000300: 8.433e0

QD
type: SiteQuality
SIO_000300: 1.309e1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 2

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

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

South Asian
type: Population
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allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
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: 10378
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499700059988002e-5
allele num: 66680
num of homozygotes: 0

QD
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MQRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

MQ
type: SiteQuality
SIO_000300: 4.074e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-1

InbreedingCoeff
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SIO_000300: 3.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.918e0

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.677e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.64e-1

DP
type: SiteQuality
SIO_000300: 2.0782e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 7
allele frequency: 1.049758555532228e-4
allele num: 66682
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
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: 5.048e0

VQSLOD
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SIO_000300: -1.819e0

MQ
type: SiteQuality
SIO_000300: 4.523e1

DP
type: SiteQuality
SIO_000300: 2.081629e6

BaseQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

QD
type: SiteQuality
SIO_000300: 1.271e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.29e-1

GenotypeQuality
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variant carriers: 20

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16492
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)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 19
allele frequency: 2.849173739615512e-4
allele num: 66686
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.976e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.94e-1

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -9.547e-1

FS
type: SiteQuality
SIO_000300: 1.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

QD
type: SiteQuality
SIO_000300: 1.189e1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66696
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
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: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 906
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South Asian
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allele frequency: 0.0e0
allele num: 16500
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VQSLOD
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QD
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InbreedingCoeff
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FS
type: SiteQuality
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MQ
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ClippingRankSum
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MQRankSum
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DP
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
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: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

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

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

Other
type: Population
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allele num: 908
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.28e-1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.923816852635629e-4
allele num: 10396
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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South Asian
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allele frequency: 0.0e0
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Other
type: Population
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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: 66716
num of homozygotes: 0

MQRankSum
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SIO_000300: 6.68e-1

DP
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FS
type: SiteQuality
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VQSLOD
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MQ
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BaseQRankSum
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ClippingRankSum
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SIO_000300: 9.68e-1

QD
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 4.496402877697842e-5
allele num: 66720
num of homozygotes: 0

East Asian
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African
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Latino
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European (Finnish)
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num of homozygotes: 0

VQSLOD
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ClippingRankSum
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BaseQRankSum
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FS
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MQ
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InbreedingCoeff
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QD
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MQRankSum
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ReadPosRankSum
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DP
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GenotypeQuality
all individuals: 1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 10398
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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.53e-1

MQ
type: SiteQuality
SIO_000300: 4.896e1

DP
type: SiteQuality
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MQRankSum
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QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.024e0

FS
type: SiteQuality
SIO_000300: 7.571e0

VQSLOD
type: SiteQuality
SIO_000300: -2.621e0

GenotypeQuality
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variant carriers: 0

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

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

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

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

African
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allele count: 8
allele frequency: 7.692307692307692e-4
allele num: 10400
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.75e0

QD
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VQSLOD
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DP
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MQ
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SIO_000300: 5.061e1

InbreedingCoeff
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SIO_000300: 0.0e0

BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
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allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

VQSLOD
type: SiteQuality
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InbreedingCoeff
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.815e0

FS
type: SiteQuality
SIO_000300: 4.952e0

BaseQRankSum
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MQRankSum
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ReadPosRankSum
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SIO_000300: 1.99e0

DP
type: SiteQuality
SIO_000300: 2.091475e6

QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
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BaseQRankSum
type: SiteQuality
SIO_000300: 5.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.64e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.87e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.77e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.585e-1

FS
type: SiteQuality
SIO_000300: 1.396e0

MQ
type: SiteQuality
SIO_000300: 5.318e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.091585e6

QD
type: SiteQuality
SIO_000300: 1.566e1

GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
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: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.91e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.56e0

MQRankSum
type: SiteQuality
SIO_000300: 2.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.15e-1

FS
type: SiteQuality
SIO_000300: 5.093e0

MQ
type: SiteQuality
SIO_000300: 5.37e1

VQSLOD
type: SiteQuality
SIO_000300: -1.672e0

DP
type: SiteQuality
SIO_000300: 2.091698e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.968e1

GenotypeQuality
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variant carriers: 55

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 2401
bin: 7.25e1
variant carriers: 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: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 54
allele frequency: 5.190311418685121e-3
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.267e1

DP
type: SiteQuality
SIO_000300: 2.098077e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.97e-1

FS
type: SiteQuality
SIO_000300: 5.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.98e0

QD
type: SiteQuality
SIO_000300: 1.526e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7196

South Asian
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allele count: 420
allele frequency: 2.543912780133253e-2
allele num: 16510
num of homozygotes: 10

African
type: Population
allele count: 2828
allele frequency: 2.717662886796079e-1
allele num: 10406
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Other
type: Population
allele count: 60
allele frequency: 6.607929515418502e-2
allele num: 908
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European (Finnish)
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allele count: 395
allele frequency: 5.972180223767765e-2
allele num: 6614
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European (Non-Finnish)
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allele count: 2216
allele frequency: 3.320646147391135e-2
allele num: 66734
num of homozygotes: 41

East Asian
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allele count: 769
allele frequency: 8.886064247746707e-2
allele num: 8654
num of homozygotes: 31

Latino
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allele count: 1032
allele frequency: 8.913456555536362e-2
allele num: 11578
num of homozygotes: 46

QD
type: SiteQuality
SIO_000300: 1.479e1

MQRankSum
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.115e1

FS
type: SiteQuality
SIO_000300: 5.3e-1

VQSLOD
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ClippingRankSum
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SIO_000300: -1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.52e-1

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

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

Other
type: Population
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East Asian
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allele frequency: 1.155535012710885e-4
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African
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele num: 11578
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
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MQ
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FS
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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QD
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ReadPosRankSum
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SIO_000300: 1.03e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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African
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Other
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European (Non-Finnish)
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East Asian
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Latino
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ClippingRankSum
type: SiteQuality
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DP
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FS
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ReadPosRankSum
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MQ
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BaseQRankSum
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VQSLOD
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MQRankSum
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

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

East Asian
type: Population
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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

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

FS
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ReadPosRankSum
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MQRankSum
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VQSLOD
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DP
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QD
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BaseQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 1.727414061150458e-4
allele num: 11578
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African
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South Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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East Asian
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BaseQRankSum
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QD
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MQ
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VQSLOD
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DP
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FS
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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Latino
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South Asian
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East Asian
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Other
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European (Finnish)
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ClippingRankSum
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BaseQRankSum
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MQ
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VQSLOD
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MQRankSum
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FS
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ReadPosRankSum
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DP
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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African
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Other
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BaseQRankSum
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QD
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FS
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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MQRankSum
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DP
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MQ
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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European (Finnish)
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African
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South Asian
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East Asian
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MQ
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DP
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MQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

East Asian
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Latino
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allele frequency: 3.454828122300915e-4
allele num: 11578
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Other
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European (Finnish)
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allele frequency: 0.0e0
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African
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South Asian
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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MQRankSum
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MQ
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ReadPosRankSum
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FS
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
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African
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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European (Finnish)
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DP
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VQSLOD
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QD
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ReadPosRankSum
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FS
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele num: 11578
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Other
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African
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European (Finnish)
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European (Non-Finnish)
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South Asian
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QD
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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FS
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MQRankSum
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VQSLOD
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MQ
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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allele frequency: 1.155535012710885e-4
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num of homozygotes: 0

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

South Asian
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European (Finnish)
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Other
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Latino
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num of homozygotes: 0

InbreedingCoeff
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DP
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MQ
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VQSLOD
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ReadPosRankSum
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MQRankSum
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FS
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QD
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Non-Finnish)
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European (Finnish)
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East Asian
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Latino
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MQ
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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FS
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ReadPosRankSum
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BaseQRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 2.996703626011388e-5
allele num: 66740
num of homozygotes: 0

South Asian
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East Asian
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African
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allele frequency: 1.921968095329617e-4
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European (Finnish)
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allele frequency: 0.0e0
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Other
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Latino
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ReadPosRankSum
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DP
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BaseQRankSum
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QD
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InbreedingCoeff
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FS
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MQRankSum
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VQSLOD
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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European (Non-Finnish)
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African
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European (Finnish)
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Latino
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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FS
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MQRankSum
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ClippingRankSum
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QD
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BaseQRankSum
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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African
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European (Finnish)
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European (Non-Finnish)
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South Asian
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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FS
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MQ
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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Latino
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South Asian
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Other
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European (Non-Finnish)
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European (Finnish)
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InbreedingCoeff
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MQ
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BaseQRankSum
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QD
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VQSLOD
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MQRankSum
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FS
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ReadPosRankSum
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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East Asian
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African
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Latino
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European (Non-Finnish)
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QD
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ReadPosRankSum
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FS
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MQRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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DP
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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European (Finnish)
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East Asian
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African
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Other
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Latino
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MQ
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FS
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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ClippingRankSum
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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Other
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European (Finnish)
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Latino
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South Asian
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DP
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InbreedingCoeff
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MQRankSum
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QD
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BaseQRankSum
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FS
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VQSLOD
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MQ
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Finnish)
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European (Non-Finnish)
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South Asian
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East Asian
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Other
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MQ
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ReadPosRankSum
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FS
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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DP
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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East Asian
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European (Finnish)
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Latino
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South Asian
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FS
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VQSLOD
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MQ
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DP
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QD
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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African
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.042e1

MQRankSum
type: SiteQuality
SIO_000300: 1.66e0

DP
type: SiteQuality
SIO_000300: 2.477421e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.428e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.847e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.79e-1

FS
type: SiteQuality
SIO_000300: 3.98e0

MQ
type: SiteQuality
SIO_000300: 5.158e1

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.394e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.83e-2

QD
type: SiteQuality
SIO_000300: 1.518e1

FS
type: SiteQuality
SIO_000300: 9.66e-1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

DP
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SIO_000300: 2.477496e6

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.5e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 8.970000000000001e0

MQ
type: SiteQuality
SIO_000300: 4.984e1

MQRankSum
type: SiteQuality
SIO_000300: -4.388e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.624e0

DP
type: SiteQuality
SIO_000300: 2.477472e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.080000000000001e-1

FS
type: SiteQuality
SIO_000300: 7.242e0

VQSLOD
type: SiteQuality
SIO_000300: -4.023e0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.477451e6

MQRankSum
type: SiteQuality
SIO_000300: -3.898e0

FS
type: SiteQuality
SIO_000300: 6.969e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.31e-1

MQ
type: SiteQuality
SIO_000300: 5.183e1

VQSLOD
type: SiteQuality
SIO_000300: -3.175e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.929e0

QD
type: SiteQuality
SIO_000300: 8.81e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.25e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6058
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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South Asian
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allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 908
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.32e-1

MQ
type: SiteQuality
SIO_000300: 5.495e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.653e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.502e0

MQRankSum
type: SiteQuality
SIO_000300: 2.49e0

QD
type: SiteQuality
SIO_000300: 1.36e1

DP
type: SiteQuality
SIO_000300: 2.477531e6

VQSLOD
type: SiteQuality
SIO_000300: -3.763e0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 8

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 2.996703626011388e-5
allele num: 66740
num of homozygotes: 0

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

South Asian
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allele frequency: 2.422480620155039e-4
allele num: 16512
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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MQRankSum
type: SiteQuality
SIO_000300: -9.07e-1

FS
type: SiteQuality
SIO_000300: 5.21e-1

BaseQRankSum
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SIO_000300: 2.3e-2

MQ
type: SiteQuality
SIO_000300: 5.234e1

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.471e1

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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