X-152128516-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152128516
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152128516
    reference: chr 0
allele count: 2
allele frequency: 1.164008846467233e-4
allele num: 17182
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.1654+35C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1700+76C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1613+76C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1700+76C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1604+76C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1427+76C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.879+76C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1607+76C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.941+76C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.908+76C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.518+76C>G
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5858
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29503
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16576
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

X-152128521-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152128521
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152128521
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 15379
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.879+81C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.1654+40C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1607+81C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1613+81C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.908+81C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.518+81C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1700+81C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.941+81C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1604+81C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1700+81C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1427+81C>A
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16926
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4926
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29207
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD

X-152128528-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152128528
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152128528
    reference: chr 0
allele count: 1
allele frequency: 7.219695328857122e-5
allele num: 13851
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1427+88G>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.879+88G>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1607+88G>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1604+88G>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.1654+47G>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.518+88G>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.941+88G>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1613+88G>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1700+88G>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.908+88G>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1700+88G>C
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

X-152132341-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132341
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132341
    reference: chr 0
allele count: 26
allele frequency: 3.627181540436099e-4
allele num: 71681
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.909-42C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1701-42C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.1655-42C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1605-42C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.519-42C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.942-42C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.880-42C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1614-42C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1701-42C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1428-42C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1608-42C>T
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15183
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2902
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12152
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7620
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10479
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5690
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4264
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD

X-152132342-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132342
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132342
    reference: chr 0
allele count: 1
allele frequency: 1.391556037961649e-5
allele num: 71862
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1701-41T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.942-41T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.880-41T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1614-41T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1605-41T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1428-41T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.1655-41T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.909-41T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1701-41T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1608-41T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.519-41T>C
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2924
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6910
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15033
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11284
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5773
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS

X-152132345-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132345
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132345
    reference: chr 0
allele count: 2
allele frequency: 2.77789352334125e-5
allele num: 71997
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.1655-38C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1614-38C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.880-38C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1701-38C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1428-38C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1701-38C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.909-38C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.519-38C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.942-38C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1605-38C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1608-38C>T
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6035
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14506
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5553
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13015
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4164
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

X-152132348-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132348
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132348
    reference: chr 0
allele count: 3
allele frequency: 4.143875352229405e-5
allele num: 72396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.942-35G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.880-35G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1614-35G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.909-35G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.1655-35G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1701-35G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1701-35G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1608-35G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1605-35G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1428-35G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.519-35G>A
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13670
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14715
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

X-152132353-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132353
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132353
    reference: chr 0
allele count: 2
allele frequency: 2.7474414451542e-5
allele num: 72795
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.909-30C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1428-30C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.880-30C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.1655-30C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1605-30C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1608-30C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1614-30C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1701-30C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1701-30C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.942-30C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.519-30C>T
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17267
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11946
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12045
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3527
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD

X-152132354-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132354
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132354
    reference: chr 0
allele count: 1
allele frequency: 1.36563515691148e-5
allele num: 73226
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1605-29G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1614-29G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1701-29G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1701-29G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.909-29G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.880-29G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1428-29G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.942-29G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.1655-29G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1608-29G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.519-29G>A
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6917
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11803
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3055
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11437
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3533
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

X-152132357-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132357
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132357
    reference: chr 0
allele count: 3
allele frequency: 4.055314489638671e-5
allele num: 73977
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1428-26C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1701-26C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1608-26C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.519-26C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.909-26C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.880-26C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.1655-26C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1614-26C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1701-26C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1605-26C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.942-26C>T
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2658
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3594
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10128
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11347
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11434
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

X-152132363-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132363
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132363
    reference: chr 0
allele count: 7
allele frequency: 9.182375086904621e-5
allele num: 76233
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1428-20C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.1655-20C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.942-20C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1605-20C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.909-20C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.880-20C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1608-20C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1701-20C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1701-20C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1614-20C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.519-20C>A
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3795
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9826
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7218
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

X-152132364-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132364
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132364
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 76614
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1608-19C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.942-19C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1614-19C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1701-19C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.880-19C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.909-19C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1605-19C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1428-19C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.1655-19C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1701-19C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.519-19C>G
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9554
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6850
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8510
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD

X-152132366-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132366
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132366
    reference: chr 0
allele count: 2
allele frequency: 2.594774124912426e-5
allele num: 77078
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1701-17C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.942-17C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.880-17C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.519-17C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1605-17C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1428-17C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.909-17C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1608-17C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1614-17C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1701-17C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.1655-17C>G
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9079
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25776
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8762
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD

X-152132369-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132369
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132369
    reference: chr 0
allele count: 25
allele frequency: 3.199836168388178e-4
allele num: 78129
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1608-14T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1701-14T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1614-14T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1428-14T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1701-14T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.519-14T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.1655-14T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.880-14T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.942-14T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1605-14T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.909-14T>C
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3955
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8264
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5349
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27326
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9161
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2302
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

X-152132371-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132371
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132371
    reference: chr 0
allele count: 1
allele frequency: 1.266704667806701e-5
allele num: 78945
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1428-12T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1608-12T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.1655-12T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.880-12T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1701-12T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1701-12T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1614-12T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.942-12T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.909-12T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1605-12T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.519-12T>C
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4665
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7643
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

X-152132372-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132372
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132372
    reference: chr 0
allele count: 30
allele frequency: 3.797131899705089e-4
allele num: 79007
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1605-11A>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.942-11A>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1701-11A>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1608-11A>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.880-11A>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.1655-11A>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1428-11A>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.909-11A>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1701-11A>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.519-11A>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1614-11A>T
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9505
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4008
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7340
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 29037
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1067
  bin: 3.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD

X-152132376-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132376
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132376
    reference: chr 0
allele count: 21
allele frequency: 2.610706382555509e-4
allele num: 80438
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.1655-7C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1608-7C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1605-7C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.909-7C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1614-7C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.519-7C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.880-7C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1428-7C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.942-7C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1701-7C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1701-7C>T
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 3491
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30956
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9925
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 3.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: c.1701-7C>T
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

X-152132386-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132386
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132386
    reference: chr 0
allele count: 1
allele frequency: 1.193773278578932e-5
allele num: 83768
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.883G>T
  hgvsp: ENST00000426821.2:c.883G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.1658G>T
  hgvsp: ENSP00000391272.2:p.Ter553LeuextTer42
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1608G>T
  hgvsp: ENST00000370268.4:c.1608G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1617G>T
  hgvsp: ENST00000539731.1:c.1617G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.945G>T
  hgvsp: ENST00000318529.8:c.945G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.912G>T
  hgvsp: ENST00000324823.6:c.912G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1704G>T
  hgvsp: ENST00000370270.2:c.1704G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1431G>T
  hgvsp: ENST00000318504.7:c.1431G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1611G>T
  hgvsp: ENST00000449285.2:c.1611G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1704G>T
  hgvsp: ENST00000535861.1:c.1704G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.522G>T
  hgvsp: ENST00000454925.1:c.522G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
canonical: false
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4251
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ter553LeuextTer42
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

X-152132387-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132387
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132387
    reference: chr 0
allele count: 1
allele frequency: 1.190858966572589e-5
allele num: 83973
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.1659A>G
  hgvsp: ENSP00000391272.2:p.Ter553TrpextTer42
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1612A>G
  hgvsp: ENSP00000395228.2:p.Arg538Gly
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.523A>G
  hgvsp: ENSP00000392984.2:p.Arg175Gly
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.913A>G
  hgvsp: ENSP00000325307.6:p.Arg305Gly
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1705A>G
  hgvsp: ENSP00000359293.2:p.Arg569Gly
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.884A>G
  hgvsp: ENSP00000409121.2:p.Arg296Gly
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1432A>G
  hgvsp: ENSP00000312782.7:p.Arg478Gly
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1609A>G
  hgvsp: ENSP00000359291.4:p.Arg537Gly
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1618A>G
  hgvsp: ENSP00000444367.1:p.Arg540Gly
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1705A>G
  hgvsp: ENSP00000440847.1:p.Arg569Gly
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.946A>G
  hgvsp: ENSP00000313919.8:p.Arg316Gly
  variant of: http://identifiers.org/hgnc/12976
canonical: false
consequence: stop lost
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4247
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35020
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11375
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ter553TrpextTer42
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

X-152132393-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132393
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132393
    reference: chr 0
allele count: 2
allele frequency: 2.353218025650076e-5
allele num: 84990
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1615C>T
  hgvsp: ENSP00000359291.4:p.Pro539Ser
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1711C>T
  hgvsp: ENSP00000359293.2:p.Pro571Ser
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1438C>T
  hgvsp: ENSP00000312782.7:p.Pro480Ser
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*6C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.890C>T
  hgvsp: ENSP00000409121.2:p.Pro298Ser
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.529C>T
  hgvsp: ENSP00000392984.2:p.Pro177Ser
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.919C>T
  hgvsp: ENSP00000325307.6:p.Pro307Ser
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.952C>T
  hgvsp: ENSP00000313919.8:p.Pro318Ser
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1711C>T
  hgvsp: ENSP00000440847.1:p.Pro571Ser
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1624C>T
  hgvsp: ENSP00000444367.1:p.Pro542Ser
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1618C>T
  hgvsp: ENSP00000395228.2:p.Pro540Ser
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11988
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro571Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

X-152132397-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132397
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132397
    reference: chr 0
allele count: 1
allele frequency: 1.169659044388561e-5
allele num: 85495
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1442C>T
  hgvsp: ENSP00000312782.7:p.Ser481Leu
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.956C>T
  hgvsp: ENSP00000313919.8:p.Ser319Leu
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1715C>T
  hgvsp: ENSP00000440847.1:p.Ser572Leu
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.533C>T
  hgvsp: ENSP00000392984.2:p.Ser178Leu
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1628C>T
  hgvsp: ENSP00000444367.1:p.Ser543Leu
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1715C>T
  hgvsp: ENSP00000359293.2:p.Ser572Leu
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*10C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.894C>T
  hgvsp: ENSP00000409121.2:p.Ser299Leu
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.923C>T
  hgvsp: ENSP00000325307.6:p.Ser308Leu
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1622C>T
  hgvsp: ENSP00000395228.2:p.Ser541Leu
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1619C>T
  hgvsp: ENSP00000359291.4:p.Ser540Leu
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36224
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser572Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

X-152132400-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132400
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132400
    reference: chr 0
allele count: 2
allele frequency: 2.327557112432646e-5
allele num: 85927
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1625G>A
  hgvsp: ENSP00000395228.2:p.Ser542Asn
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.926G>A
  hgvsp: ENSP00000325307.6:p.Ser309Asn
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.897G>A
  hgvsp: ENSP00000409121.2:p.Ser300Asn
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1445G>A
  hgvsp: ENSP00000312782.7:p.Ser482Asn
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.536G>A
  hgvsp: ENSP00000392984.2:p.Ser179Asn
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1622G>A
  hgvsp: ENSP00000359291.4:p.Ser541Asn
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1631G>A
  hgvsp: ENSP00000444367.1:p.Ser544Asn
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*13G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1718G>A
  hgvsp: ENSP00000359293.2:p.Ser573Asn
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1718G>A
  hgvsp: ENSP00000440847.1:p.Ser573Asn
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.959G>A
  hgvsp: ENSP00000313919.8:p.Ser320Asn
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12626
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser573Asn
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

X-152132407-GGTCACTGTTACT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132407
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132395
    reference: chr 0
allele count: 1
allele frequency: 1.157019056103854e-5
allele num: 86429
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsp: ENSP00000359291.4:p.Val546_Thr549del
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsp: ENSP00000444367.1:p.Val549_Thr552del
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsp: ENSP00000409121.2:p.Val305_Thr308del
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsp: ENSP00000392984.2:p.Val184_Thr187del
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsp: ENSP00000440847.1:p.Val578_Thr581del
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsp: ENSP00000312782.7:p.Val487_Thr490del
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsp: ENSP00000395228.2:p.Val547_Thr550del
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsp: ENSP00000359293.2:p.Val578_Thr581del
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsp: ENSP00000325307.6:p.Val314_Thr317del
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsp: ENSP00000313919.8:p.Val325_Thr328del
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4422
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1877
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val578_Thr581del
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: GGTCACTGTTACT
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

X-152132418-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132418
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132418
    reference: chr 0
allele count: 2
allele frequency: 2.306326252911737e-5
allele num: 86718
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*31C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.977C>T
  hgvsp: ENSP00000313919.8:p.Thr326Ile
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1736C>T
  hgvsp: ENSP00000359293.2:p.Thr579Ile
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1463C>T
  hgvsp: ENSP00000312782.7:p.Thr488Ile
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1640C>T
  hgvsp: ENSP00000359291.4:p.Thr547Ile
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.915C>T
  hgvsp: ENSP00000409121.2:p.Thr306Ile
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.944C>T
  hgvsp: ENSP00000325307.6:p.Thr315Ile
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1643C>T
  hgvsp: ENSP00000395228.2:p.Thr548Ile
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.554C>T
  hgvsp: ENSP00000392984.2:p.Thr185Ile
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1736C>T
  hgvsp: ENSP00000440847.1:p.Thr579Ile
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1649C>T
  hgvsp: ENSP00000444367.1:p.Thr550Ile
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37173
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4450
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13316
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr579Ile
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

X-152132421-T-TCACTGC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132421
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132427
    reference: chr 0
allele count: 2
allele frequency: 2.305103499147112e-5
allele num: 86764
alternate allele: TCACTGC
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1470_1475dupTGCCAC
  hgvsp: ENSP00000312782.7:p.Ala491_Thr492dup
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.561_566dupTGCCAC
  hgvsp: ENSP00000392984.2:p.Ala188_Thr189dup
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1743_1748dupTGCCAC
  hgvsp: ENSP00000440847.1:p.Ala582_Thr583dup
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.951_956dupTGCCAC
  hgvsp: ENSP00000325307.6:p.Ala318_Thr319dup
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1656_1661dupTGCCAC
  hgvsp: ENSP00000444367.1:p.Ala553_Thr554dup
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1650_1655dupTGCCAC
  hgvsp: ENSP00000395228.2:p.Ala551_Thr552dup
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1647_1652dupTGCCAC
  hgvsp: ENSP00000359291.4:p.Ala550_Thr551dup
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1743_1748dupTGCCAC
  hgvsp: ENSP00000359293.2:p.Ala582_Thr583dup
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.922_927dupTGCCAC
  hgvsp: ENSP00000409121.2:p.Ala309_Thr310dup
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*38_*43dupTGCCAC
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.984_989dupTGCCAC
  hgvsp: ENSP00000313919.8:p.Ala329_Thr330dup
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: inframe insertion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37169
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13378
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala582_Thr583dup
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD

X-152132435-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132435
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132435
    reference: chr 0
allele count: 1
allele frequency: 1.151092386674954e-5
allele num: 86874
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1660G>A
  hgvsp: ENSP00000395228.2:p.Glu554Lys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.994G>A
  hgvsp: ENSP00000313919.8:p.Glu332Lys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.961G>A
  hgvsp: ENSP00000325307.6:p.Glu321Lys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1753G>A
  hgvsp: ENSP00000440847.1:p.Glu585Lys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1666G>A
  hgvsp: ENSP00000444367.1:p.Glu556Lys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*48G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1753G>A
  hgvsp: ENSP00000359293.2:p.Glu585Lys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.932G>A
  hgvsp: ENSP00000409121.2:p.Glu312Lys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.571G>A
  hgvsp: ENSP00000392984.2:p.Glu191Lys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1657G>A
  hgvsp: ENSP00000359291.4:p.Glu553Lys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1480G>A
  hgvsp: ENSP00000312782.7:p.Glu494Lys
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4473
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu585Lys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

X-152132443-TCA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132443
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132441
    reference: chr 0
allele count: 1
allele frequency: 1.150747986191024e-5
allele num: 86900
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1677_1678delCA
  hgvsp: ENSP00000444367.1:p.Ile560LeufsTer8
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1764_1765delCA
  hgvsp: ENSP00000359293.2:p.Ile589LeufsTer8
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1491_1492delCA
  hgvsp: ENSP00000312782.7:p.Ile498LeufsTer8
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1764_1765delCA
  hgvsp: ENSP00000440847.1:p.Ile589LeufsTer8
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.943_944delCA
  hgvsp: ENSP00000409121.2:p.Ile316LeufsTer8
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1671_1672delCA
  hgvsp: ENSP00000395228.2:p.Ile558LeufsTer8
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.582_583delCA
  hgvsp: ENSP00000392984.2:p.Ile195LeufsTer8
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1668_1669delCA
  hgvsp: ENSP00000359291.4:p.Ile557LeufsTer8
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1005_1006delCA
  hgvsp: ENSP00000313919.8:p.Ile336LeufsTer8
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.972_973delCA
  hgvsp: ENSP00000325307.6:p.Ile325LeufsTer8
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*59_*60delCA
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4470
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37040
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile589LeufsTer8
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
reference allele: TCA
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

X-152132455-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132455
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132455
    reference: chr 0
allele count: 4
allele frequency: 4.603945581363229e-5
allele num: 86882
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1014T>A
  hgvsp: ENST00000318529.8:c.1014T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1686T>A
  hgvsp: ENST00000539731.1:c.1686T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.591T>A
  hgvsp: ENST00000454925.1:c.591T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1680T>A
  hgvsp: ENST00000449285.2:c.1680T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*68T>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1773T>A
  hgvsp: ENST00000370270.2:c.1773T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.981T>A
  hgvsp: ENST00000324823.6:c.981T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1677T>A
  hgvsp: ENST00000370268.4:c.1677T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.952T>A
  hgvsp: ENST00000426821.2:c.952T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1500T>A
  hgvsp: ENST00000318504.7:c.1500T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1773T>A
  hgvsp: ENST00000535861.1:c.1773T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36902
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13741
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4477
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ile591Ile
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

X-152132459-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132459
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132460
    reference: chr 0
allele count: 1
allele frequency: 1.151264664233661e-5
allele num: 86861
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1509dupC
  hgvsp: ENSP00000312782.7:p.Ala504ArgfsTer3
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1686dupC
  hgvsp: ENSP00000359291.4:p.Ala563ArgfsTer3
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1023dupC
  hgvsp: ENSP00000313919.8:p.Ala342ArgfsTer3
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.961dupC
  hgvsp: ENSP00000409121.2:p.Ala322ArgfsTer3
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1695dupC
  hgvsp: ENSP00000444367.1:p.Ala566ArgfsTer3
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1782dupC
  hgvsp: ENSP00000359293.2:p.Ala595ArgfsTer3
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1689dupC
  hgvsp: ENSP00000395228.2:p.Ala564ArgfsTer3
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.990dupC
  hgvsp: ENSP00000325307.6:p.Ala331ArgfsTer3
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*77dupC
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.600dupC
  hgvsp: ENSP00000392984.2:p.Ala201ArgfsTer3
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1782dupC
  hgvsp: ENSP00000440847.1:p.Ala595ArgfsTer3
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13772
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4479
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala595ArgfsTer3
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum

X-152132460-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132460
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132460
    reference: chr 0
allele count: 1
allele frequency: 1.151277918489523e-5
allele num: 86860
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1685C>T
  hgvsp: ENSP00000395228.2:p.Ala562Val
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.986C>T
  hgvsp: ENSP00000325307.6:p.Ala329Val
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1682C>T
  hgvsp: ENSP00000359291.4:p.Ala561Val
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.957C>T
  hgvsp: ENSP00000409121.2:p.Ala320Val
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1019C>T
  hgvsp: ENSP00000313919.8:p.Ala340Val
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*73C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1778C>T
  hgvsp: ENSP00000440847.1:p.Ala593Val
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1778C>T
  hgvsp: ENSP00000359293.2:p.Ala593Val
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1691C>T
  hgvsp: ENSP00000444367.1:p.Ala564Val
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1505C>T
  hgvsp: ENSP00000312782.7:p.Ala502Val
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.596C>T
  hgvsp: ENSP00000392984.2:p.Ala199Val
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36764
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13786
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala593Val
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

X-152132462-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132462
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132462
    reference: chr 0
allele count: 1
allele frequency: 1.151436993367723e-5
allele num: 86848
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1687C>G
  hgvsp: ENSP00000395228.2:p.Pro563Ala
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1780C>G
  hgvsp: ENSP00000359293.2:p.Pro594Ala
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.959C>G
  hgvsp: ENSP00000409121.2:p.Pro321Ala
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1507C>G
  hgvsp: ENSP00000312782.7:p.Pro503Ala
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1693C>G
  hgvsp: ENSP00000444367.1:p.Pro565Ala
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1684C>G
  hgvsp: ENSP00000359291.4:p.Pro562Ala
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.598C>G
  hgvsp: ENSP00000392984.2:p.Pro200Ala
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.988C>G
  hgvsp: ENSP00000325307.6:p.Pro330Ala
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*75C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1780C>G
  hgvsp: ENSP00000440847.1:p.Pro594Ala
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1021C>G
  hgvsp: ENSP00000313919.8:p.Pro341Ala
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13819
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro594Ala
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

X-152132464-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132464
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132464
    reference: chr 0
allele count: 9
allele frequency: 1.036603625809127e-4
allele num: 86822
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.990C>T
  hgvsp: ENST00000324823.6:c.990C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1782C>T
  hgvsp: ENST00000370270.2:c.1782C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1023C>T
  hgvsp: ENST00000318529.8:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.961C>T
  hgvsp: ENST00000426821.2:c.961C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1695C>T
  hgvsp: ENST00000539731.1:c.1695C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.600C>T
  hgvsp: ENST00000454925.1:c.600C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1689C>T
  hgvsp: ENST00000449285.2:c.1689C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*77C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1509C>T
  hgvsp: ENST00000318504.7:c.1509C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1686C>T
  hgvsp: ENST00000370268.4:c.1686C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1782C>T
  hgvsp: ENST00000535861.1:c.1782C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro594Pro
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP

X-152132465-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132465
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132465
    reference: chr 0
allele count: 8
allele frequency: 9.214891264283081e-5
allele num: 86816
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.991G>A
  hgvsp: ENSP00000325307.6:p.Ala331Thr
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1024G>A
  hgvsp: ENSP00000313919.8:p.Ala342Thr
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*78G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1783G>A
  hgvsp: ENSP00000359293.2:p.Ala595Thr
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1687G>A
  hgvsp: ENSP00000359291.4:p.Ala563Thr
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1696G>A
  hgvsp: ENSP00000444367.1:p.Ala566Thr
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1510G>A
  hgvsp: ENSP00000312782.7:p.Ala504Thr
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.962G>A
  hgvsp: ENSP00000409121.2:p.Ala322Thr
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1690G>A
  hgvsp: ENSP00000395228.2:p.Ala564Thr
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.601G>A
  hgvsp: ENSP00000392984.2:p.Ala201Thr
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1783G>A
  hgvsp: ENSP00000440847.1:p.Ala595Thr
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13821
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36513
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala595Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

X-152132481-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132481
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132481
    reference: chr 0
allele count: 1
allele frequency: 1.156764760318342e-5
allele num: 86448
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1799C>G
  hgvsp: ENSP00000359293.2:p.Ser600Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1706C>G
  hgvsp: ENSP00000395228.2:p.Ser569Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1040C>G
  hgvsp: ENSP00000313919.8:p.Ser347Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.617C>G
  hgvsp: ENSP00000392984.2:p.Ser206Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.978C>G
  hgvsp: ENSP00000409121.2:p.Ser327Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1703C>G
  hgvsp: ENSP00000359291.4:p.Ser568Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1799C>G
  hgvsp: ENSP00000440847.1:p.Ser600Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1526C>G
  hgvsp: ENSP00000312782.7:p.Ser509Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1712C>G
  hgvsp: ENSP00000444367.1:p.Ser571Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*94C>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1007C>G
  hgvsp: ENSP00000325307.6:p.Ser336Cys
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35360
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13645
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser600Cys
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD

X-152132487-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132487
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132487
    reference: chr 0
allele count: 1
allele frequency: 1.159164937578968e-5
allele num: 86269
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.984C>G
  hgvsp: ENSP00000409121.2:p.Ser329Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1013C>G
  hgvsp: ENSP00000325307.6:p.Ser338Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1532C>G
  hgvsp: ENSP00000312782.7:p.Ser511Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1805C>G
  hgvsp: ENSP00000359293.2:p.Ser602Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1718C>G
  hgvsp: ENSP00000444367.1:p.Ser573Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1709C>G
  hgvsp: ENSP00000359291.4:p.Ser570Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.623C>G
  hgvsp: ENSP00000392984.2:p.Ser208Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1805C>G
  hgvsp: ENSP00000440847.1:p.Ser602Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1046C>G
  hgvsp: ENSP00000313919.8:p.Ser349Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1712C>G
  hgvsp: ENSP00000395228.2:p.Ser571Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*100C>G
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34674
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser602Cys
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum

X-152132493-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132493
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132493
    reference: chr 0
allele count: 3
allele frequency: 3.488615484801265e-5
allele num: 85994
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1715C>T
  hgvsp: ENSP00000359291.4:p.Thr572Ile
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1019C>T
  hgvsp: ENSP00000325307.6:p.Thr340Ile
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1724C>T
  hgvsp: ENSP00000444367.1:p.Thr575Ile
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1538C>T
  hgvsp: ENSP00000312782.7:p.Thr513Ile
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.629C>T
  hgvsp: ENSP00000392984.2:p.Thr210Ile
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1811C>T
  hgvsp: ENSP00000359293.2:p.Thr604Ile
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1811C>T
  hgvsp: ENSP00000440847.1:p.Thr604Ile
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1718C>T
  hgvsp: ENSP00000395228.2:p.Thr573Ile
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*106C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.990C>T
  hgvsp: ENSP00000409121.2:p.Thr331Ile
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1052C>T
  hgvsp: ENSP00000313919.8:p.Thr351Ile
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33395
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr604Ile
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS

X-152132501-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132501
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132501
    reference: chr 0
allele count: 1
allele frequency: 1.168715815062409e-5
allele num: 85564
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.990+8G>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.629+8G>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1724+8G>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1052+8G>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1538+8G>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1019+8G>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*106+8G>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1715+8G>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1811+8G>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1718+8G>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1811+8G>C
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4864
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30680
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12662
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1811+8G>C
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-152132505-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132505
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132505
    reference: chr 0
allele count: 1
allele frequency: 1.170548987475126e-5
allele num: 85430
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*106+12T>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.629+12T>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.990+12T>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1724+12T>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1718+12T>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1715+12T>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1538+12T>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1811+12T>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1811+12T>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1019+12T>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1052+12T>G
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4292
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12334
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29532
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5807
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

X-152132506-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132506
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132506
    reference: chr 0
allele count: 29
allele frequency: 3.39618222274271e-4
allele num: 85390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1019+13A>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1715+13A>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1538+13A>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*106+13A>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1718+13A>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1052+13A>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1724+13A>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.990+13A>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1811+13A>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.629+13A>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1811+13A>G
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29142
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12167
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1029
  bin: 3.75e1
  variant carriers: 2
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum

X-152132512-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132512
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132512
    reference: chr 0
allele count: 4
allele frequency: 4.703392321712035e-5
allele num: 85045
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1811+19C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1538+19C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1019+19C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1052+19C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1718+19C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.990+19C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1715+19C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*106+19C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.629+19C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1811+19C>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1724+19C>A
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8051
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26229
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4258
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

X-152132520-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132520
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132520
    reference: chr 0
allele count: 1
allele frequency: 1.179453912838356e-5
allele num: 84785
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1724+27G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1538+27G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1052+27G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1019+27G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.990+27G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1811+27G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*106+27G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1715+27G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1718+27G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1811+27G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.629+27G>T
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9919
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6576
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

X-152132532-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132532
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132532
    reference: chr 0
allele count: 574
allele frequency: 6.852504029129111e-3
allele num: 83765
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1811+39C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1019+39C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1715+39C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1538+39C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.990+39C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1718+39C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.629+39C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1811+39C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1724+39C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*106+39C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1052+39C>T
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10536
  bin: 1.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 9522
  bin: 2.75e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 2669
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 16846
  bin: 2.25e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 11531
  bin: 1.75e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 4.25e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4163
  bin: 3.25e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 9.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 3.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 5717
  bin: 3.25e1
  variant carriers: 12
num of homozygotes: 2
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP

X-152132533-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152132533
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152132533
    reference: chr 0
allele count: 5558
allele frequency: 6.686235353559657e-2
allele num: 83126
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1019+40G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1718+40G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.629+40G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1715+40G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*106+40G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1811+40G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1811+40G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.990+40G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1538+40G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1724+40G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1052+40G>A
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11770
  bin: 1.75e1
  variant carriers: 752
genotype depth: GenotypeDepth
  all individuals: 2760
  bin: 7.5e0
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 3.75e1
  variant carriers: 579
genotype depth: GenotypeDepth
  all individuals: 4245
  bin: 3.25e1
  variant carriers: 672
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 4.25e1
  variant carriers: 485
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 15376
  bin: 2.25e1
  variant carriers: 800
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 5.25e1
  variant carriers: 191
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 10608
  bin: 1.25e1
  variant carriers: 439
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.75e1
  variant carriers: 351
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 8949
  bin: 2.75e1
  variant carriers: 637
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 9.75e1
  variant carriers: 221
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.75e1
  variant carriers: 144
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 41
genotype quality: GenotypeQuality
  all individuals: 5598
  bin: 3.25e1
  variant carriers: 139
num of homozygotes: 171
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

X-152133955-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152133955
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152133955
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 16876
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1812-36G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1725-36G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1716-36G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1719-36G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*107-36G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1053-36G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1020-36G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.991-36G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1539-36G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.630-36G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1812-36G>T
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8787
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32592
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 766
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

X-152133958-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152133958
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152133958
    reference: chr 0
allele count: 1
allele frequency: 5.887894488930759e-5
allele num: 16984
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1716-33G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.630-33G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1812-33G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1725-33G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1719-33G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1812-33G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.991-33G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1020-33G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1053-33G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1539-33G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*107-33G>A
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32445
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 961
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

X-152133965-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152133965
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152133965
    reference: chr 0
allele count: 2
allele frequency: 1.155201293825449e-4
allele num: 17313
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1539-26T>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1020-26T>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*107-26T>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1719-26T>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1812-26T>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1812-26T>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1716-26T>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.991-26T>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1053-26T>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.630-26T>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1725-26T>G
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10372
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31985
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 813
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum

X-152133970-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152133970
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152133970
    reference: chr 0
allele count: 1
allele frequency: 5.707111060381235e-5
allele num: 17522
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1719-21T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1020-21T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*107-21T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.630-21T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1053-21T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1812-21T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.991-21T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1539-21T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1716-21T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1725-21T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1812-21T>C
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31224
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3078
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11723
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD

X-152133995-G-GGGATT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152133995
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152134000
    reference: chr 0
allele count: 1
allele frequency: 5.012782595618828e-5
allele num: 19949
alternate allele: GGGATT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1058_1062dupGGATT
  hgvsp: ENSP00000313919.8:p.Leu355GlyfsTer5
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*112_*116dupGGATT
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1817_1821dupGGATT
  hgvsp: ENSP00000440847.1:p.Leu608GlyfsTer5
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1544_1548dupGGATT
  hgvsp: ENSP00000312782.7:p.Leu517GlyfsTer5
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.996_1000dupGGATT
  hgvsp: ENSP00000409121.2:p.Leu335GlyfsTer5
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1025_1029dupGGATT
  hgvsp: ENSP00000325307.6:p.Leu344GlyfsTer5
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1817_1821dupGGATT
  hgvsp: ENSP00000359293.2:p.Leu608GlyfsTer5
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1730_1734dupGGATT
  hgvsp: ENSP00000444367.1:p.Leu579GlyfsTer5
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1724_1728dupGGATT
  hgvsp: ENSP00000395228.2:p.Leu577GlyfsTer5
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1721_1725dupGGATT
  hgvsp: ENSP00000359291.4:p.Leu576GlyfsTer5
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.635_639dupGGATT
  hgvsp: ENSP00000392984.2:p.Leu214GlyfsTer5
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4930
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24481
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu608GlyfsTer5
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP

X-152133998-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152133998
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152133998
    reference: chr 0
allele count: 1
allele frequency: 4.931452805996646e-5
allele num: 20278
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1546A>G
  hgvsp: ENSP00000312782.7:p.Ile516Val
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1819A>G
  hgvsp: ENSP00000359293.2:p.Ile607Val
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1726A>G
  hgvsp: ENSP00000395228.2:p.Ile576Val
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1723A>G
  hgvsp: ENSP00000359291.4:p.Ile575Val
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1732A>G
  hgvsp: ENSP00000444367.1:p.Ile578Val
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1060A>G
  hgvsp: ENSP00000313919.8:p.Ile354Val
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*114A>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.998A>G
  hgvsp: ENSP00000409121.2:p.Ile334Val
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1027A>G
  hgvsp: ENSP00000325307.6:p.Ile343Val
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1819A>G
  hgvsp: ENSP00000440847.1:p.Ile607Val
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.637A>G
  hgvsp: ENSP00000392984.2:p.Ile213Val
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23766
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20822
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile607Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

X-152134003-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152134003
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152134003
    reference: chr 0
allele count: 2
allele frequency: 9.602919287463389e-5
allele num: 20827
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1065C>T
  hgvsp: ENST00000318529.8:c.1065C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*119C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1824C>T
  hgvsp: ENST00000535861.1:c.1824C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.1003C>T
  hgvsp: ENST00000426821.2:c.1003C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1728C>T
  hgvsp: ENST00000370268.4:c.1728C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1737C>T
  hgvsp: ENST00000539731.1:c.1737C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.642C>T
  hgvsp: ENST00000454925.1:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1551C>T
  hgvsp: ENST00000318504.7:c.1551C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1731C>T
  hgvsp: ENST00000449285.2:c.1731C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1824C>T
  hgvsp: ENST00000370270.2:c.1824C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1032C>T
  hgvsp: ENST00000324823.6:c.1032C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22103
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22502
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu608Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

X-152134007-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152134007
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152134007
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 21471
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1555G>A
  hgvsp: ENSP00000312782.7:p.Val519Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1741G>A
  hgvsp: ENSP00000444367.1:p.Val581Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1069G>A
  hgvsp: ENSP00000313919.8:p.Val357Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1828G>A
  hgvsp: ENSP00000359293.2:p.Val610Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1036G>A
  hgvsp: ENSP00000325307.6:p.Val346Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1732G>A
  hgvsp: ENSP00000359291.4:p.Val578Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1828G>A
  hgvsp: ENSP00000440847.1:p.Val610Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.1007G>A
  hgvsp: ENSP00000409121.2:p.Val337Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*123G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1735G>A
  hgvsp: ENSP00000395228.2:p.Val579Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.646G>A
  hgvsp: ENSP00000392984.2:p.Val216Met
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23203
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21319
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val610Met
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: QD

X-152134016-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152134016
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152134016
    reference: chr 0
allele count: 1
allele frequency: 4.445629945763315e-5
allele num: 22494
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1837T>C
  hgvsp: ENSP00000440847.1:p.Tyr613His
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1078T>C
  hgvsp: ENSP00000313919.8:p.Tyr360His
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.1016T>C
  hgvsp: ENSP00000409121.2:p.Tyr340His
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1564T>C
  hgvsp: ENSP00000312782.7:p.Tyr522His
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1744T>C
  hgvsp: ENSP00000395228.2:p.Tyr582His
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1837T>C
  hgvsp: ENSP00000359293.2:p.Tyr613His
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1750T>C
  hgvsp: ENSP00000444367.1:p.Tyr584His
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1741T>C
  hgvsp: ENSP00000359291.4:p.Tyr581His
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*132T>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.655T>C
  hgvsp: ENSP00000392984.2:p.Tyr219His
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1045T>C
  hgvsp: ENSP00000325307.6:p.Tyr349His
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19781
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5870
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24408
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr613His
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

X-152134018-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152134018
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152134018
    reference: chr 0
allele count: 46
allele frequency: 2.028397565922921e-3
allele num: 22678
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1839C>T
  hgvsp: ENST00000370270.2:c.1839C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1752C>T
  hgvsp: ENST00000539731.1:c.1752C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1566C>T
  hgvsp: ENST00000318504.7:c.1566C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1746C>T
  hgvsp: ENST00000449285.2:c.1746C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1047C>T
  hgvsp: ENST00000324823.6:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1743C>T
  hgvsp: ENST00000370268.4:c.1743C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.1018C>T
  hgvsp: ENST00000426821.2:c.1018C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1080C>T
  hgvsp: ENST00000318529.8:c.1080C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1839C>T
  hgvsp: ENST00000535861.1:c.1839C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.657C>T
  hgvsp: ENST00000454925.1:c.657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*134C>T
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24616
  bin: 7.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19542
  bin: 2.5e0
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5897
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Tyr613Tyr
num of homozygotes: 1
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

X-152134019-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152134019
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152134019
    reference: chr 0
allele count: 14
allele frequency: 6.156552330694811e-4
allele num: 22740
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1048G>A
  hgvsp: ENSP00000325307.6:p.Val350Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.658G>A
  hgvsp: ENSP00000392984.2:p.Val220Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.1019G>A
  hgvsp: ENSP00000409121.2:p.Val341Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1567G>A
  hgvsp: ENSP00000312782.7:p.Val523Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1840G>A
  hgvsp: ENSP00000440847.1:p.Val614Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1744G>A
  hgvsp: ENSP00000359291.4:p.Val582Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1747G>A
  hgvsp: ENSP00000395228.2:p.Val583Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1840G>A
  hgvsp: ENSP00000359293.2:p.Val614Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*135G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1753G>A
  hgvsp: ENSP00000444367.1:p.Val585Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1081G>A
  hgvsp: ENSP00000313919.8:p.Val361Met
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19640
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5815
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24403
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val614Met
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

X-152134021-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152134021
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152134021
    reference: chr 0
allele count: 1
allele frequency: 4.362430746411901e-5
allele num: 22923
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1569G>C
  hgvsp: ENST00000318504.7:c.1569G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1050G>C
  hgvsp: ENST00000324823.6:c.1050G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1746G>C
  hgvsp: ENST00000370268.4:c.1746G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1749G>C
  hgvsp: ENST00000449285.2:c.1749G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.1021G>C
  hgvsp: ENST00000426821.2:c.1021G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1083G>C
  hgvsp: ENST00000318529.8:c.1083G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1842G>C
  hgvsp: ENST00000370270.2:c.1842G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1842G>C
  hgvsp: ENST00000535861.1:c.1842G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*137G>C
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.660G>C
  hgvsp: ENST00000454925.1:c.660G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1755G>C
  hgvsp: ENST00000539731.1:c.1755G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19410
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24645
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val614Val
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

X-152134031-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152134031
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152134031
    reference: chr 0
allele count: 3
allele frequency: 1.267802053839327e-4
allele num: 23663
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1756G>A
  hgvsp: ENSP00000359291.4:p.Glu586Lys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1852G>A
  hgvsp: ENSP00000440847.1:p.Glu618Lys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1579G>A
  hgvsp: ENSP00000312782.7:p.Glu527Lys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1765G>A
  hgvsp: ENSP00000444367.1:p.Glu589Lys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1093G>A
  hgvsp: ENSP00000313919.8:p.Glu365Lys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1852G>A
  hgvsp: ENSP00000359293.2:p.Glu618Lys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.1031G>A
  hgvsp: ENSP00000409121.2:p.Glu345Lys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1060G>A
  hgvsp: ENSP00000325307.6:p.Glu354Lys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1759G>A
  hgvsp: ENSP00000395228.2:p.Glu587Lys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.670G>A
  hgvsp: ENSP00000392984.2:p.Glu224Lys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*147G>A
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18601
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25212
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu618Lys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD

X-152134034-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152134034
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152134034
    reference: chr 0
allele count: 1
allele frequency: 4.203623523477237e-5
allele num: 23789
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.673G>A
  hgvsp: ENSP00000392984.2:p.Val225Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1855G>A
  hgvsp: ENSP00000359293.2:p.Val619Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1582G>A
  hgvsp: ENSP00000312782.7:p.Val528Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1855G>A
  hgvsp: ENSP00000440847.1:p.Val619Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.1034G>A
  hgvsp: ENSP00000409121.2:p.Val346Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1063G>A
  hgvsp: ENSP00000325307.6:p.Val355Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1762G>A
  hgvsp: ENSP00000395228.2:p.Val588Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1759G>A
  hgvsp: ENSP00000359291.4:p.Val587Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1096G>A
  hgvsp: ENSP00000313919.8:p.Val366Met
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*150G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1768G>A
  hgvsp: ENSP00000444367.1:p.Val590Met
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5989
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18799
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24915
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val619Met
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-152134042-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152134042
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152134042
    reference: chr 0
allele count: 1
allele frequency: 4.165104752384522e-5
allele num: 24009
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1590T>A
  hgvsp: ENST00000318504.7:c.1590T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1776T>A
  hgvsp: ENST00000539731.1:c.1776T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1863T>A
  hgvsp: ENST00000370270.2:c.1863T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1767T>A
  hgvsp: ENST00000370268.4:c.1767T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1863T>A
  hgvsp: ENST00000535861.1:c.1863T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*158T>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1104T>A
  hgvsp: ENST00000318529.8:c.1104T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.1042T>A
  hgvsp: ENST00000426821.2:c.1042T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1071T>A
  hgvsp: ENST00000324823.6:c.1071T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1770T>A
  hgvsp: ENST00000449285.2:c.1770T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.681T>A
  hgvsp: ENST00000454925.1:c.681T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5900
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19048
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser621Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

X-152134061-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152134061
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152134061
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 23740
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1090C>T
  hgvsp: ENSP00000325307.6:p.Arg364Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1795C>T
  hgvsp: ENSP00000444367.1:p.Arg599Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.1061C>T
  hgvsp: ENSP00000409121.2:p.Arg355Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1882C>T
  hgvsp: ENSP00000359293.2:p.Arg628Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1786C>T
  hgvsp: ENSP00000359291.4:p.Arg596Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1123C>T
  hgvsp: ENSP00000313919.8:p.Arg375Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1789C>T
  hgvsp: ENSP00000395228.2:p.Arg597Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1882C>T
  hgvsp: ENSP00000440847.1:p.Arg628Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.700C>T
  hgvsp: ENSP00000392984.2:p.Arg234Cys
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*177C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1609C>T
  hgvsp: ENSP00000312782.7:p.Arg537Cys
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19888
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22735
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4911
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg628Cys
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-152134066-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152134066
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152134066
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 23468
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1095T>C
  hgvsp: ENST00000324823.6:c.1095T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1791T>C
  hgvsp: ENST00000370268.4:c.1791T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.1066T>C
  hgvsp: ENST00000426821.2:c.1066T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1794T>C
  hgvsp: ENST00000449285.2:c.1794T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1800T>C
  hgvsp: ENST00000539731.1:c.1800T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.705T>C
  hgvsp: ENST00000454925.1:c.705T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1128T>C
  hgvsp: ENST00000318529.8:c.1128T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1614T>C
  hgvsp: ENST00000318504.7:c.1614T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1887T>C
  hgvsp: ENST00000370270.2:c.1887T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1887T>C
  hgvsp: ENST00000535861.1:c.1887T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*182T>C
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4640
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23952
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18542
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr629Tyr
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

X-152134072-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152134072
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152134072
    reference: chr 0
allele count: 1
allele frequency: 4.46149727848666e-5
allele num: 22414
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1133+1G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1805+1G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.710+1G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1796+1G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*187+1G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1892+1G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.1071+1G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1100+1G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1892+1G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1619+1G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1799+1G>A
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15709
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26307
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1484
  bin: 2.5e0
  variant carriers: 0
hgvs: c.1892+1G>A
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

X-152134074-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152134074
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152134074
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 22541
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1799+3A>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.1071+3A>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1796+3A>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1619+3A>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*187+3A>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1892+3A>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1133+3A>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1892+3A>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1805+3A>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.710+3A>G
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1100+3A>G
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15662
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3957
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26408
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1892+3A>G
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

X-152134079-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152134079
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152134079
    reference: chr 0
allele count: 1
allele frequency: 4.584001833600734e-5
allele num: 21815
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*187+8C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1796+8C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1619+8C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1892+8C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1799+8C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1805+8C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.710+8C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1133+8C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1100+8C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.1071+8C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1892+8C>T
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27433
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3212
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1892+8C>T
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

X-152134080-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152134080
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152134080
    reference: chr 0
allele count: 1
allele frequency: 4.60045084418273e-5
allele num: 21737
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.1071+9G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1100+9G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1619+9G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1796+9G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1133+9G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1892+9G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1799+9G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1892+9G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.710+9G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1805+9G>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*187+9G>A
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27689
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14081
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

X-152134082-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152134082
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152134082
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 21575
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.710+11G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1892+11G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1799+11G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1892+11G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1100+11G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.1071+11G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1133+11G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1619+11G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*187+11G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1796+11G>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1805+11G>T
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 13517
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28145
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3430
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27370
  bin: 7.5e0
  variant carriers: 1
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD

X-152134083-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152134083
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152134083
    reference: chr 0
allele count: 1
allele frequency: 4.678362573099416e-5
allele num: 21375
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1892+12T>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1619+12T>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*187+12T>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.710+12T>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1799+12T>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.1071+12T>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1100+12T>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1892+12T>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1133+12T>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1796+12T>A
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1805+12T>A
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28536
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12990
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3321
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

X-152134092-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152134092
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152134092
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 20264
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.710+21C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1619+21C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.1071+21C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1100+21C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1799+21C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1892+21C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1133+21C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1892+21C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1805+21C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1796+21C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*187+21C>T
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10467
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3319
  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

X-152134096-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24152134096
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24152134096
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 19690
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000395228
  ensembl transcript: ENST00000449285
  gene symbol: ZNF185
  hgvsc: ENST00000449285.2:c.1799+25C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000391272
  ensembl transcript: ENST00000436731
  gene symbol: ZNF185
  hgvsc: ENST00000436731.2:c.*187+25C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000409121
  ensembl transcript: ENST00000426821
  gene symbol: ZNF185
  hgvsc: ENST00000426821.2:c.1071+25C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000392984
  ensembl transcript: ENST00000454925
  gene symbol: ZNF185
  hgvsc: ENST00000454925.1:c.710+25C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359291
  ensembl transcript: ENST00000370268
  gene symbol: ZNF185
  hgvsc: ENST00000370268.4:c.1796+25C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000312782
  ensembl transcript: ENST00000318504
  gene symbol: ZNF185
  hgvsc: ENST00000318504.7:c.1619+25C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000359293
  ensembl transcript: ENST00000370270
  gene symbol: ZNF185
  hgvsc: ENST00000370270.2:c.1892+25C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000440847
  ensembl transcript: ENST00000535861
  gene symbol: ZNF185
  hgvsc: ENST00000535861.1:c.1892+25C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000325307
  ensembl transcript: ENST00000324823
  gene symbol: ZNF185
  hgvsc: ENST00000324823.6:c.1100+25C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000444367
  ensembl transcript: ENST00000539731
  gene symbol: ZNF185
  hgvsc: ENST00000539731.1:c.1805+25C>T
  variant of: http://identifiers.org/hgnc/12976
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147394
  ensembl protein: ENSP00000313919
  ensembl transcript: ENST00000318529
  gene symbol: ZNF185
  hgvsc: ENST00000318529.8:c.1133+25C>T
  variant of: http://identifiers.org/hgnc/12976
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9838
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30376
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28237
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

X-152134100-TCG-T
type: Variant
allele count: 1
allele frequency: 5.203996669442132e-5
allele num: 19216
alternate allele: T
canonical: true
consequence: intron
filter: PASS
num of homozygotes: 0
reference allele: TCG

GenotypeQuality
all individuals: 122
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1158
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4170
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 60
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28845
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2173
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11718
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1118
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3266
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1170
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.875468867216804e-4
allele num: 10664
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1611
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 819
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2337
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 688
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 918
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 145
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

QD
type: SiteQuality
SIO_000300: 1.055e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.277e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

DP
type: SiteQuality
SIO_000300: 3.56374e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.64e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.34e-1

GenotypeQuality
all individuals: 1143
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4892
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27595
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1120
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8633
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3191
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 237
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5085
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 805
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1545
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 678
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2163
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 570
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 711
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 134
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.83e1

DP
type: SiteQuality
SIO_000300: 3.39104e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.29e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

GenotypeQuality
all individuals: 208
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6585
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5698
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 89
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1127
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6365
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1064
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25973
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4374
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1443
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 492
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.151675688126224e-4
allele num: 8683
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 585
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1952
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 128
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.33e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.244e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.58e-2

DP
type: SiteQuality
SIO_000300: 3.33001e5

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e0

QD
type: SiteQuality
SIO_000300: 1.455e1

GenotypeQuality
all individuals: 1221
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1663
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1211
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6516
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3529
bin: 9.75e1
variant carriers: 19

GenotypeQuality
all individuals: 10135
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2272
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1368
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2883
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10757
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1478
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5241
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1155
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1600
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 527
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3297
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 644
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5840
num of homozygotes: 0

African
type: Population
allele count: 25
allele frequency: 3.52013517319065e-3
allele num: 7102
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4001
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5689
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.207437816952427e-4
allele num: 8282
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40257
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.43e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.524e0

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.130986e6

QD
type: SiteQuality
SIO_000300: 1.693e1

GenotypeQuality
all individuals: 2149
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1678
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 645
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4009
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 511
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5694
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8311
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7095
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.704158145875937e-4
allele num: 5868
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40374
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.743e1

DP
type: SiteQuality
SIO_000300: 1.13757e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.62e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 965
bin: 1.75e1
variant carriers: 0

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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.47237125126709e-5
allele num: 40447
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.405678942929435e-4
allele num: 7114
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8322
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5685
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4018
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5899
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -6.64e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -9.2e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

DP
type: SiteQuality
SIO_000300: 1.156093e6

QD
type: SiteQuality
SIO_000300: 1.788e1

GenotypeQuality
all individuals: 4307
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1223
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1449
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 7.375719132615431e-5
allele num: 40674
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8337
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7131
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4030
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 515
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5746
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5963
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.247e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.002e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.172e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.29e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

DP
type: SiteQuality
SIO_000300: 1.176038e6

GenotypeQuality
all individuals: 3714
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1819
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GenotypeQuality
all individuals: 1494
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 516
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.660853678790899e-4
allele num: 6021
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.447441200225165e-5
allele num: 40859
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5804
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7159
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4042
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.413e0

FS
type: SiteQuality
SIO_000300: 1.741e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

DP
type: SiteQuality
SIO_000300: 1.211555e6

MQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.381e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.95e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

QD
type: SiteQuality
SIO_000300: 5.65e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 18813
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41105
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4060
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.714971702966901e-4
allele num: 5831
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7183
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8423
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 519
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6105
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.405e0

VQSLOD
type: SiteQuality
SIO_000300: -7.355e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.389e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.04e-1

QD
type: SiteQuality
SIO_000300: 9.91e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.191e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

DP
type: SiteQuality
SIO_000300: 1.225173e6

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7226
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4097
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 521
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.394433129667345e-4
allele num: 5892
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8474
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6218
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.40679679414667e-5
allele num: 41549
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.77e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.923e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.73e-1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -7.98e-1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.254356e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1962
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.153269519086611e-4
allele num: 8671
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6654
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 8.156606851549756e-4
allele num: 7356
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6058
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 531
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4165
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42798
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.87e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 3.5e-3

BaseQRankSum
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FS
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.558e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2908
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1338
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43022
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7372
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8699
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4180
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6086
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6718
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 537
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.196e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.48e-1

DP
type: SiteQuality
SIO_000300: 1.330748e6

MQRankSum
type: SiteQuality
SIO_000300: 3.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

QD
type: SiteQuality
SIO_000300: 3.047e1

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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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7383
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6127
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4207
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6832
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.144295686005264e-4
allele num: 8739
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43251
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.855287569573284e-3
allele num: 539
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.619e0

FS
type: SiteQuality
SIO_000300: 9.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.051e0

MQRankSum
type: SiteQuality
SIO_000300: 8.68e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.59e-1

DP
type: SiteQuality
SIO_000300: 1.347026e6

QD
type: SiteQuality
SIO_000300: 1.573e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 19

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1999
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variant carriers: 1

GenotypeQuality
all individuals: 2023
bin: 2.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4244
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 9.401020682245501e-4
allele num: 7446
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 543
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 4.107900862659181e-4
allele num: 43818
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7069
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6200
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8809
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.917e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.02e0

QD
type: SiteQuality
SIO_000300: 5.14e0

MQ
type: SiteQuality
SIO_000300: 5.484e1

VQSLOD
type: SiteQuality
SIO_000300: -1.661e1

FS
type: SiteQuality
SIO_000300: 5.6225e1

MQRankSum
type: SiteQuality
SIO_000300: -8.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.371283e6

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2029
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4267
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7491
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 549
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44280
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6250
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8871
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.381788033715628e-4
allele num: 7237
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.21e0

MQRankSum
type: SiteQuality
SIO_000300: -9.85e-1

DP
type: SiteQuality
SIO_000300: 1.389343e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e-1

QD
type: SiteQuality
SIO_000300: 1.226e1

GenotypeQuality
all individuals: 97
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
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variant carriers: 1

GenotypeQuality
all individuals: 2005
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 1871
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3530
bin: 9.75e1
variant carriers: 24

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4276
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6262
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8870
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 21
allele frequency: 4.742226136440621e-4
allele num: 44283
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7282
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 1.203208556149733e-3
allele num: 7480
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.735e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.469e0

MQRankSum
type: SiteQuality
SIO_000300: -1.644e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.784e0

MQ
type: SiteQuality
SIO_000300: 5.652e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.16e0

FS
type: SiteQuality
SIO_000300: 5.5767e1

DP
type: SiteQuality
SIO_000300: 1.398568e6

QD
type: SiteQuality
SIO_000300: 5.51e0

GenotypeDepth
all individuals: 203
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 17

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6340
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8960
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 3.110903717529943e-4
allele num: 45003
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 568
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4339
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 9.2702953251225e-4
allele num: 7551
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.53e0

FS
type: SiteQuality
SIO_000300: 4.6965e1

MQRankSum
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DP
type: SiteQuality
SIO_000300: 1.429986e6

InbreedingCoeff
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SIO_000300: 2.0e-3

BaseQRankSum
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SIO_000300: -2.459e0

QD
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SIO_000300: 7.92e0

ReadPosRankSum
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SIO_000300: -2.724e0

VQSLOD
type: SiteQuality
SIO_000300: -1.545e1

MQ
type: SiteQuality
SIO_000300: 5.631e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1818
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7713
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8753
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4449
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.144082332761578e-5
allele num: 46640
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6491
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
allele count: 0
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.1e-2

DP
type: SiteQuality
SIO_000300: 1.50222e6

InbreedingCoeff
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SIO_000300: 4.8e-3

ClippingRankSum
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FS
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MQ
type: SiteQuality
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VQSLOD
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MQRankSum
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SIO_000300: 5.15e-1

BaseQRankSum
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SIO_000300: -5.073e0

QD
type: SiteQuality
SIO_000300: 1.64e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 643
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7724
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9147
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46726
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6496
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 592
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 1.132246376811594e-4
allele num: 8832
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.69e0

VQSLOD
type: SiteQuality
SIO_000300: -3.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.46e-2

DP
type: SiteQuality
SIO_000300: 1.507067e6

QD
type: SiteQuality
SIO_000300: 2.141e1

MQ
type: SiteQuality
SIO_000300: 5.955e1

FS
type: SiteQuality
SIO_000300: 4.202e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.546e0

MQRankSum
type: SiteQuality
SIO_000300: 1.91e-1

GenotypeDepth
all individuals: 116
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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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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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 2110
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

South Asian
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allele count: 2
allele frequency: 2.162629757785467e-4
allele num: 9248
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9204
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7774
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 601
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4485
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47144
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.749e0

DP
type: SiteQuality
SIO_000300: 1.530292e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.91e-1

InbreedingCoeff
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SIO_000300: 1.68e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.355e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

QD
type: SiteQuality
SIO_000300: 2.583e1

GenotypeDepth
all individuals: 73
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variant carriers: 0

GenotypeQuality
all individuals: 105
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
all individuals: 129
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9466
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9225
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.112200067590402e-5
allele num: 47344
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7795
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 605
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.212e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.9e-2

QD
type: SiteQuality
SIO_000300: 2.923e1

MQ
type: SiteQuality
SIO_000300: 5.981e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.071e0

VQSLOD
type: SiteQuality
SIO_000300: -2.291e0

MQRankSum
type: SiteQuality
SIO_000300: -3.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.389999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.543313e6

GenotypeDepth
all individuals: 232
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1273
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 604
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variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9238
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.207868714496107e-5
allele num: 47530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9647
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4513
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7819
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.71e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.377e0

FS
type: SiteQuality
SIO_000300: 9.531000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 7.4e-1

QD
type: SiteQuality
SIO_000300: 1.673e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e0

DP
type: SiteQuality
SIO_000300: 1.552947e6

GenotypeQuality
all individuals: 109
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 88
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GenotypeQuality
all individuals: 2130
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 605
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GenotypeQuality
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GenotypeQuality
all individuals: 100
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GenotypeQuality
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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: 3581
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1422
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.517680983457277e-4
allele num: 6589
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47714
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9865
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7858
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 611
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

FS
type: SiteQuality
SIO_000300: 1.01e1

MQ
type: SiteQuality
SIO_000300: 5.911e1

DP
type: SiteQuality
SIO_000300: 1.565035e6

BaseQRankSum
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SIO_000300: 2.86e0

VQSLOD
type: SiteQuality
SIO_000300: 2.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.89e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

QD
type: SiteQuality
SIO_000300: 6.24e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.93e-1

GenotypeDepth
all individuals: 109
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 15
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3579
bin: 9.75e1
variant carriers: 2

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7882
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9279
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.182000669120107e-5
allele num: 47824
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9995
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6595
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4526
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

DP
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.017e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.41e-1

BaseQRankSum
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SIO_000300: -1.732e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-2

GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10014
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47844
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7885
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4526
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.154708037060978e-4
allele num: 9282
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.685e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.4e-2

BaseQRankSum
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.66e-1

MQ
type: SiteQuality
SIO_000300: 5.39e1

QD
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SIO_000300: 6.93e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1423
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.513775355737209e-4
allele num: 6606
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9296
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10034
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47890
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.2e-2

MQ
type: SiteQuality
SIO_000300: 5.972e1

DP
type: SiteQuality
SIO_000300: 1.57747e6

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 9.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.509e0

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.252e1

GenotypeDepth
all individuals: 81
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2151
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 313
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 708
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3576
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5566
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1900
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43798
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1420
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6609
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10036
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4529
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.087639088954302e-5
allele num: 47901
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 619
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9301
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7905
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.94e1

FS
type: SiteQuality
SIO_000300: 1.814e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.18e-2

QD
type: SiteQuality
SIO_000300: 3.231e1

MQRankSum
type: SiteQuality
SIO_000300: 8.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.076e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-1

DP
type: SiteQuality
SIO_000300: 1.578189e6

VQSLOD
type: SiteQuality
SIO_000300: 1.17e0

GenotypeDepth
all individuals: 109
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3579
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 96
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1905
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43675
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 70
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2144
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1424
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5566
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7905
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9303
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4529
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 3.992414412616029e-4
allele num: 10019
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47900
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.942e1

FS
type: SiteQuality
SIO_000300: 2.224e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.29e-2

QD
type: SiteQuality
SIO_000300: 1.384e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.322e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.301e0

DP
type: SiteQuality
SIO_000300: 1.577756e6

MQRankSum
type: SiteQuality
SIO_000300: 5.07e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

VQSLOD
type: SiteQuality
SIO_000300: 7.8e-1

GenotypeDepth
all individuals: 368
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2142
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3578
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1895
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
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variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 613
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variant carriers: 0

GenotypeQuality
all individuals: 43598
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5543
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variant carriers: 0

GenotypeQuality
all individuals: 1424
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4529
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6607
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10005
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.265182186234818e-4
allele num: 7904
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9303
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47895
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e-1

QD
type: SiteQuality
SIO_000300: 5.13e0

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

FS
type: SiteQuality
SIO_000300: 4.378e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.044e0

MQRankSum
type: SiteQuality
SIO_000300: -3.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

DP
type: SiteQuality
SIO_000300: 1.577428e6

MQ
type: SiteQuality
SIO_000300: 5.969e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.373e0

GenotypeDepth
all individuals: 312
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1422
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 613
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variant carriers: 0

GenotypeQuality
all individuals: 2145
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 74
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variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1895
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 419
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variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5542
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3578
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 704
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43624
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10005
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7902
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4529
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.087944210130705e-5
allele num: 47894
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.323e0

DP
type: SiteQuality
SIO_000300: 1.577667e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.18e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.52e-1

QD
type: SiteQuality
SIO_000300: 2.081e1

MQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

MQ
type: SiteQuality
SIO_000300: 5.912e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.19e-1

GenotypeDepth
all individuals: 73
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1420
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
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variant carriers: 0

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

GenotypeQuality
all individuals: 1890
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5554
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2145
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3578
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 703
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43607
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6607
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9996
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9303
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.088075003654131e-5
allele num: 47891
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4529
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 5.32e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.17e-1

DP
type: SiteQuality
SIO_000300: 1.576861e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.167e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.19e-1

FS
type: SiteQuality
SIO_000300: 2.475e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.158e0

GenotypeDepth
all individuals: 233
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
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variant carriers: 0

GenotypeQuality
all individuals: 3585
bin: 9.75e1
variant carriers: 9

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

GenotypeQuality
all individuals: 1418
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5545
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 68
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variant carriers: 0

GenotypeQuality
all individuals: 67
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variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
all individuals: 703
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2141
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1884
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43487
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.075384449940854e-4
allele num: 9299
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4529
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.003604325190228e-4
allele num: 9988
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.265502404454569e-4
allele num: 7902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 8.354044401745996e-5
allele num: 47881
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.06e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.403e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.22e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.96e-2

QD
type: SiteQuality
SIO_000300: 1.916e1

FS
type: SiteQuality
SIO_000300: 1.169e0

DP
type: SiteQuality
SIO_000300: 1.57656e6

GenotypeDepth
all individuals: 4504
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2129
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 73
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variant carriers: 0

GenotypeQuality
all individuals: 102
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variant carriers: 0

GenotypeQuality
all individuals: 1882
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variant carriers: 0

GenotypeQuality
all individuals: 116
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 1419
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 71
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
all individuals: 3582
bin: 9.75e1
variant carriers: 7

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 609
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 703
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.088554720133668e-5
allele num: 47880
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7902
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 4.006410256410256e-4
allele num: 9984
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.225806451612903e-4
allele num: 9300
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e-1

BaseQRankSum
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SIO_000300: -2.411e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

FS
type: SiteQuality
SIO_000300: 1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.61e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.6e-2

DP
type: SiteQuality
SIO_000300: 1.576622e6

VQSLOD
type: SiteQuality
SIO_000300: 2.24e0

QD
type: SiteQuality
SIO_000300: 1.379e1

GenotypeDepth
all individuals: 73
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 331
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GenotypeQuality
all individuals: 69
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GenotypeQuality
all individuals: 1325
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GenotypeQuality
all individuals: 17
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GenotypeQuality
all individuals: 104
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GenotypeQuality
all individuals: 607
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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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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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3579
bin: 9.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7878
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6601
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9277
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47752
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4515
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 615
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.019367991845056e-4
allele num: 9810
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.84e-2

DP
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SIO_000300: 1.561948e6

QD
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SIO_000300: 3.142e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.2e0

GenotypeDepth
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9729
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9272
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.097843416967358e-5
allele num: 47668
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
allele count: 0
allele frequency: 0.0e0
allele num: 612
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4514
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.896e1

BaseQRankSum
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SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: 1.38e0

ClippingRankSum
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SIO_000300: -1.38e0

DP
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MQ
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SIO_000300: 6.0e1

VQSLOD
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SIO_000300: -2.031e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.65e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9621
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.206452698439406e-5
allele num: 47546
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6593
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 611
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9254
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.27258844489692e-4
allele num: 7858
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4511
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.85e0

ReadPosRankSum
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SIO_000300: 1.3e0

MQ
type: SiteQuality
SIO_000300: 5.93e1

MQRankSum
type: SiteQuality
SIO_000300: 9.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.43e-2

DP
type: SiteQuality
SIO_000300: 1.539158e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.41e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.7e-1

QD
type: SiteQuality
SIO_000300: 1.639e1

FS
type: SiteQuality
SIO_000300: 6.131e0

GenotypeDepth
all individuals: 81
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 417
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GenotypeQuality
all individuals: 1287
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4500
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9214
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.054185114906177e-4
allele num: 9486
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6573
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 609
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47342
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.018e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.08e-2

VQSLOD
type: SiteQuality
SIO_000300: -9.744e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.501568e6

FS
type: SiteQuality
SIO_000300: 1.101e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.5e-1

GenotypeQuality
all individuals: 254
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variant carriers: 1

GenotypeQuality
all individuals: 1387
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 1535
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9204
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 605
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.275835672365399e-4
allele num: 7838
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47279
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.387e1

BaseQRankSum
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SIO_000300: 1.6e0

VQSLOD
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SIO_000300: -1.616e0

ReadPosRankSum
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SIO_000300: 9.01e-1

MQ
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SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.900000000000001e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.08e-1

DP
type: SiteQuality
SIO_000300: 1.485661e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 23
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GenotypeQuality
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GenotypeQuality
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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: 25

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 702
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variant carriers: 0

East Asian
type: Population
allele count: 27
allele frequency: 4.113972268779522e-3
allele num: 6563
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.652892561983471e-3
allele num: 605
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9200
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7832
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.060445387062566e-4
allele num: 9430
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47264
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.536e1

BaseQRankSum
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SIO_000300: 2.65e0

VQSLOD
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SIO_000300: 2.69e0

InbreedingCoeff
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SIO_000300: 7.95e-2

MQRankSum
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MQ
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SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: -1.41e-1

FS
type: SiteQuality
SIO_000300: 1.582e0

DP
type: SiteQuality
SIO_000300: 1.481142e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e-1

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 4.297840335231546e-4
allele num: 9307
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47109
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9179
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 603
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7818
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4477
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.15e-1

QD
type: SiteQuality
SIO_000300: 1.485e1

VQSLOD
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FS
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SIO_000300: 1.127e0

BaseQRankSum
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SIO_000300: -3.308e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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SIO_000300: -7.9e-1

DP
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SIO_000300: 1.447246e6

InbreedingCoeff
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SIO_000300: 6.7e-3

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 685
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6533
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4469
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7797
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9169
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9241
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.128655966622675e-5
allele num: 46978
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.52e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.407335e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

QD
type: SiteQuality
SIO_000300: 9.34e0

FS
type: SiteQuality
SIO_000300: 2.879e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.032e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

VQSLOD
type: SiteQuality
SIO_000300: 2.61e-1

GenotypeQuality
all individuals: 1672
bin: 7.25e1
variant carriers: 6

GenotypeQuality
all individuals: 705
bin: 9.25e1
variant carriers: 7

GenotypeQuality
all individuals: 178
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 909
bin: 5.25e1
variant carriers: 22

GenotypeQuality
all individuals: 343
bin: 5.75e1
variant carriers: 11

GenotypeQuality
all individuals: 2001
bin: 7.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1367
bin: 8.25e1
variant carriers: 8

GenotypeQuality
all individuals: 3738
bin: 2.75e1
variant carriers: 10

GenotypeQuality
all individuals: 1768
bin: 4.25e1
variant carriers: 16

GenotypeQuality
all individuals: 7650
bin: 2.25e1
variant carriers: 12

GenotypeQuality
all individuals: 4629
bin: 3.75e1
variant carriers: 16

GenotypeQuality
all individuals: 336
bin: 1.25e1
variant carriers: 5

GenotypeQuality
all individuals: 472
bin: 7.5e0
variant carriers: 4

GenotypeQuality
all individuals: 479
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1868
bin: 4.75e1
variant carriers: 20

GenotypeQuality
all individuals: 17914
bin: 6.25e1
variant carriers: 22

GenotypeQuality
all individuals: 3916
bin: 9.75e1
variant carriers: 384

GenotypeQuality
all individuals: 595
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4222
bin: 6.75e1
variant carriers: 25

African
type: Population
allele count: 11
allele frequency: 1.421005038108771e-3
allele num: 7741
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.242655303879794e-4
allele num: 8918
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 487
allele frequency: 1.047694856183981e-2
allele num: 46483
num of homozygotes: 2

Other
type: Population
allele count: 5
allele frequency: 8.417508417508417e-3
allele num: 594
num of homozygotes: 0

Latino
type: Population
allele count: 14
allele frequency: 1.538461538461538e-3
allele num: 9100
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6490
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 55
allele frequency: 1.239017796801081e-2
allele num: 4439
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.795e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.56e-1

QD
type: SiteQuality
SIO_000300: 1.895e1

VQSLOD
type: SiteQuality
SIO_000300: 1.964e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.372639e6

GenotypeQuality
all individuals: 1880
bin: 4.75e1
variant carriers: 213

GenotypeQuality
all individuals: 6541
bin: 9.75e1
variant carriers: 3482

GenotypeQuality
all individuals: 1819
bin: 7.75e1
variant carriers: 100

GenotypeQuality
all individuals: 476
bin: 1.25e1
variant carriers: 62

GenotypeQuality
all individuals: 3867
bin: 6.75e1
variant carriers: 183

GenotypeQuality
all individuals: 3678
bin: 2.75e1
variant carriers: 83

GenotypeQuality
all individuals: 866
bin: 5.25e1
variant carriers: 265

GenotypeQuality
all individuals: 352
bin: 2.5e0
variant carriers: 43

GenotypeQuality
all individuals: 1250
bin: 8.25e1
variant carriers: 104

GenotypeQuality
all individuals: 7483
bin: 2.25e1
variant carriers: 83

GenotypeQuality
all individuals: 669
bin: 9.25e1
variant carriers: 53

GenotypeQuality
all individuals: 646
bin: 1.75e1
variant carriers: 60

GenotypeQuality
all individuals: 443
bin: 5.75e1
variant carriers: 122

GenotypeQuality
all individuals: 596
bin: 7.5e0
variant carriers: 61

GenotypeQuality
all individuals: 1812
bin: 4.25e1
variant carriers: 144

GenotypeQuality
all individuals: 510
bin: 8.75e1
variant carriers: 23

GenotypeQuality
all individuals: 4595
bin: 3.75e1
variant carriers: 192

GenotypeQuality
all individuals: 1521
bin: 7.25e1
variant carriers: 76

GenotypeQuality
all individuals: 15876
bin: 6.25e1
variant carriers: 202

African
type: Population
allele count: 85
allele frequency: 1.099611901681759e-2
allele num: 7730
num of homozygotes: 1

Latino
type: Population
allele count: 259
allele frequency: 2.863460475400774e-2
allele num: 9045
num of homozygotes: 3

European (Non-Finnish)
type: Population
allele count: 4440
allele frequency: 9.644416447639942e-2
allele num: 46037
num of homozygotes: 147

European (Finnish)
type: Population
allele count: 554
allele frequency: 1.264551472266606e-1
allele num: 4381
num of homozygotes: 18

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6475
num of homozygotes: 0

Other
type: Population
allele count: 42
allele frequency: 7.106598984771574e-2
allele num: 591
num of homozygotes: 1

South Asian
type: Population
allele count: 178
allele frequency: 2.00744332919815e-2
allele num: 8867
num of homozygotes: 1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.22e-1

DP
type: SiteQuality
SIO_000300: 1.421185e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.33e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.582e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.36e0

QD
type: SiteQuality
SIO_000300: 1.937e1

GenotypeQuality
all individuals: 4705
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1000
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2163
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 810
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3316
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3325
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 26217
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1747
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5777
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4188
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 367
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2149
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1089
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 170
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8321
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 1.166e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.36e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

DP
type: SiteQuality
SIO_000300: 5.66499e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 238
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6148
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2329
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26517
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3145
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1745
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 738
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4349
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3325
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 56
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1100
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2172
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4204
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 5.882352941176471e-3
allele num: 170
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8374
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 370
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.279999999999999e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

VQSLOD
type: SiteQuality
SIO_000300: -2.176e0

DP
type: SiteQuality
SIO_000300: 5.71225e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.962e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e0

QD
type: SiteQuality
SIO_000300: 8.6e0

GenotypeQuality
all individuals: 7860
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 149
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2573
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 751
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27544
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3060
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 638
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1529
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3211
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3324
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 541
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4291
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.349348055914484e-4
allele num: 8513
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1124
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2199
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 174
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.94e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.95e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.36e1

DP
type: SiteQuality
SIO_000300: 5.89892e5

VQSLOD
type: SiteQuality
SIO_000300: -2.748e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.46e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.58e0

GenotypeQuality
all individuals: 27637
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 712
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1588
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2138
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2657
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9254
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3325
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3496
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 673
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8637
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4324
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 4.496402877697842e-4
allele num: 2224
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 174
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 636
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1135
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 392
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.96e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.81e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.034e0

VQSLOD
type: SiteQuality
SIO_000300: -1.407e0

DP
type: SiteQuality
SIO_000300: 6.04487e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.458e1

GenotypeDepth
all individuals: 95
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 844
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1302
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
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variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 949
bin: 2.5e0
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GenotypeQuality
all individuals: 142
bin: 8.75e1
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GenotypeQuality
all individuals: 3325
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23434
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18464
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5927
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 876
bin: 1.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9885
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 187
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 530
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.106593638087213e-4
allele num: 4747
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2472
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1280
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.59e1

MQ
type: SiteQuality
SIO_000300: 3.266e1

VQSLOD
type: SiteQuality
SIO_000300: 3.42e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.44e-2

DP
type: SiteQuality
SIO_000300: 6.93848e5

GenotypeDepth
all individuals: 169
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22695
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6020
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1684
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18873
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variant carriers: 0

GenotypeQuality
all individuals: 936
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 864
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 80
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GenotypeQuality
all individuals: 3325
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10055
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2501
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1301
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 193
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4778
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.757469244288225e-3
allele num: 569
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 881
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.471e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.56e-1

FS
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SIO_000300: 0.0e0

MQRankSum
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SIO_000300: -1.533e0

QD
type: SiteQuality
SIO_000300: 2.49e1

MQ
type: SiteQuality
SIO_000300: 5.928e1

DP
type: SiteQuality
SIO_000300: 7.00998e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.29e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -9.61e-1

GenotypeDepth
all individuals: 1934
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1768
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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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variant carriers: 1

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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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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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 953
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4826
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 199
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.933114247052001e-4
allele num: 10346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1331
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.734e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.48e-1

QD
type: SiteQuality
SIO_000300: 1.145e1

VQSLOD
type: SiteQuality
SIO_000300: 7.94e-1

DP
type: SiteQuality
SIO_000300: 7.14937e5

BaseQRankSum
type: SiteQuality
SIO_000300: -9.55e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.12e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 319
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3323
bin: 9.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 679
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4885
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1030
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 205
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10696
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1362
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.81e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.84e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.27656e5

QD
type: SiteQuality
SIO_000300: 1.426e1

GenotypeDepth
all individuals: 138
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variant carriers: 0

GenotypeQuality
all individuals: 60
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 900
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variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 7.122507122507123e-4
allele num: 1404
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11266
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1181
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 789
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4929
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2719
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.634e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.333e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.78e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.585e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.66e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.44356e5

GenotypeDepth
all individuals: 400
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 109
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variant carriers: 1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 31

GenotypeQuality
all individuals: 18982
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variant carriers: 10

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6955
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 305
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 902
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 122
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 394
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variant carriers: 2

GenotypeQuality
all individuals: 396
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 145
bin: 8.75e1
variant carriers: 6

GenotypeQuality
all individuals: 259
bin: 8.25e1
variant carriers: 4

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1191
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1413
num of homozygotes: 0

South Asian
type: Population
allele count: 45
allele frequency: 9.078071414161792e-3
allele num: 4957
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2735
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 207
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 8.805142203046579e-5
allele num: 11357
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-1

DP
type: SiteQuality
SIO_000300: 7.48237e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.52e-1

QD
type: SiteQuality
SIO_000300: 1.751e1

MQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.580000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-2

GenotypeDepth
all individuals: 954
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variant carriers: 5

GenotypeQuality
all individuals: 65
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3331
bin: 9.75e1
variant carriers: 14

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

African
type: Population
allele count: 14
allele frequency: 5.092761004001455e-3
allele num: 2749
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1198
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4951
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1425
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 205
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.89e-1

QD
type: SiteQuality
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VQSLOD
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ReadPosRankSum
type: SiteQuality
SIO_000300: -4.4e-1

InbreedingCoeff
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SIO_000300: -3.58e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.25e-1

DP
type: SiteQuality
SIO_000300: 7.47143e5

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 392
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 205
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1222
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.018570851836899e-4
allele num: 4954
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1427
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 853
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.219e0

MQRankSum
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BaseQRankSum
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FS
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QD
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MQ
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SIO_000300: 5.929e1

ReadPosRankSum
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DP
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SIO_000300: 7.49659e5

ClippingRankSum
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InbreedingCoeff
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SIO_000300: -3.59e-2

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 647
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GenotypeQuality
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GenotypeQuality
all individuals: 63
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GenotypeQuality
all individuals: 336
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variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 3.22234156820623e-3
allele num: 931
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11910
num of homozygotes: 0

East 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: 220
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2859
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -1.573e-1

ClippingRankSum
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BaseQRankSum
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MQRankSum
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SIO_000300: 5.31e-1

FS
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SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: 2.82e-2

ReadPosRankSum
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SIO_000300: -3.61e-1

DP
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SIO_000300: 7.60317e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.117e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele frequency: 2.010454362685967e-4
allele num: 4974
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1320
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 222
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 11970
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 951
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2866
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 7.58749e5

MQRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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SIO_000300: -6.879999999999999e-1

QD
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SIO_000300: 2.499e1

MQ
type: SiteQuality
SIO_000300: 5.963e1

VQSLOD
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SIO_000300: -4.107e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.72e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Non-Finnish)
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allele count: 1
allele frequency: 8.248783304462591e-5
allele num: 12123
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 count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 218
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 count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e-1

QD
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.9e-1

FS
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SIO_000300: 2.522e0

BaseQRankSum
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SIO_000300: 1.16e0

MQRankSum
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SIO_000300: -1.157e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.51e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.435e0

DP
type: SiteQuality
SIO_000300: 7.58546e5

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4933
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1309
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 936
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 11977
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1502
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 218
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 7.25872e5

MQRankSum
type: SiteQuality
SIO_000300: -1.927e0

VQSLOD
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SIO_000300: -2.214e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.22e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e-1

QD
type: SiteQuality
SIO_000300: 1.462e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.363e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2848
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 222
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 922
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 1262
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 4908
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 11832
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: -2.252e-1

DP
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SIO_000300: 7.13134e5

FS
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SIO_000300: 0.0e0

QD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -4.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 2741
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 8.890469416785207e-5
allele num: 11248
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 215
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 4813
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
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QD
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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DP
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FS
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SIO_000300: 8.77e-1

MQ
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 0

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

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

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

European (Finnish)
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allele frequency: 0.0e0
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Latino
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African
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Other
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QD
type: SiteQuality
SIO_000300: 1.583e1

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

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 9.407337723424271e-4
allele num: 1063
num of homozygotes: 0

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

African
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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: 737
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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Other
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allele frequency: 0.0e0
allele num: 210
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DP
type: SiteQuality
SIO_000300: 6.69139e5

ClippingRankSum
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MQ
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FS
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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QD
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MQRankSum
type: SiteQuality
SIO_000300: 9.19e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.093e0

GenotypeQuality
all individuals: 577
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1310
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1693
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4731
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12872
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26987
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1356
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3320
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 760
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.371742112482853e-3
allele num: 729
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2679
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1038
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1373
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4761
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10946
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 211
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.83e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.34e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.080000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.346e1

MQRankSum
type: SiteQuality
SIO_000300: 3.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.81e0

VQSLOD
type: SiteQuality
SIO_000300: -1.261e0

DP
type: SiteQuality
SIO_000300: 6.65735e5

GenotypeQuality
all individuals: 3320
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12313
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1702
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1414
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1280
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4543
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2656
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 702
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1036
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10862
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1365
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 210
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4744
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.58709e5

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.37e-2

QD
type: SiteQuality
SIO_000300: 1.205e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.8e0

GenotypeQuality
all individuals: 63
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1518
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1448
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27604
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1874
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11492
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4300
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 204
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1028
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1346
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2640
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4731
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 671
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 9.298000929800093e-5
allele num: 10755
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-2

QD
type: SiteQuality
SIO_000300: 1.121e1

DP
type: SiteQuality
SIO_000300: 6.52594e5

MQRankSum
type: SiteQuality
SIO_000300: -5.3e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.1e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.298e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.12e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 638
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8577
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1229
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2719
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1987
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28495
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3209
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10174
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 197
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 595
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1303
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 867
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.591e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.93e-2

DP
type: SiteQuality
SIO_000300: 6.19674e5

VQSLOD
type: SiteQuality
SIO_000300: 2.06e-1

GenotypeQuality
all individuals: 135
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3257
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2701
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2249
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 814
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1284
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 881
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7448
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3320
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 111
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 555
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4583
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9848
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 189
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2433
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1288
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -7.605e-1

FS
type: SiteQuality
SIO_000300: 6.455e0

QD
type: SiteQuality
SIO_000300: 1.129e1

MQ
type: SiteQuality
SIO_000300: 5.739e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.054e0

MQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.73e-1

DP
type: SiteQuality
SIO_000300: 6.06731e5

ClippingRankSum
type: SiteQuality
SIO_000300: 5.73e-1