7-148876489-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876489
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876489
    reference: chr 7
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1012C>T
  hgvsp: ENSP00000338984.4:p.Arg338Cys
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1525C>T
  hgvsp: ENSP00000420418.1:p.Arg509Cys
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1012C>T
  hgvsp: ENSP00000416751.2:p.Arg338Cys
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1540C>T
  hgvsp: ENSP00000439340.1:p.Arg514Cys
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1012C>T
  hgvsp: ENSP00000419391.1:p.Arg338Cys
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1012C>T
  hgvsp: ENSP00000418564.1:p.Arg338Cys
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1012C>T
  hgvsp: ENSP00000389972.2:p.Arg338Cys
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11912
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10292
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2634
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39905
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg509Cys
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

7-148876497-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876497
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876497
    reference: chr 7
allele count: 2
allele frequency: 1.649049323065253e-5
allele num: 121282
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1020C>T
  hgvsp: ENST00000420008.2:c.1020C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1533C>T
  hgvsp: ENST00000475153.1:c.1533C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1020C>T
  hgvsp: ENST00000483892.1:c.1020C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1020C>T
  hgvsp: ENST00000491174.1:c.1020C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1020C>T
  hgvsp: ENST00000426851.2:c.1020C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1548C>T
  hgvsp: ENST00000540950.1:c.1548C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1020C>T
  hgvsp: ENST00000335901.4:c.1020C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13000
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2919
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2043
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2634
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Tyr511Tyr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

7-148876512-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876512
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876512
    reference: chr 7
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1035C>T
  hgvsp: ENST00000426851.2:c.1035C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1035C>T
  hgvsp: ENST00000335901.4:c.1035C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1035C>T
  hgvsp: ENST00000491174.1:c.1035C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1035C>T
  hgvsp: ENST00000483892.1:c.1035C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1563C>T
  hgvsp: ENST00000540950.1:c.1563C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1548C>T
  hgvsp: ENST00000475153.1:c.1548C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1035C>T
  hgvsp: ENST00000420008.2:c.1035C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28610
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13017
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40212
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1264
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Cys516Cys
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

7-148876530-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876530
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876530
    reference: chr 7
allele count: 2
allele frequency: 1.648587160803192e-5
allele num: 121316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1581C>T
  hgvsp: ENST00000540950.1:c.1581C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1566C>T
  hgvsp: ENST00000475153.1:c.1566C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1053C>T
  hgvsp: ENST00000335901.4:c.1053C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1053C>T
  hgvsp: ENST00000426851.2:c.1053C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1053C>T
  hgvsp: ENST00000491174.1:c.1053C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1053C>T
  hgvsp: ENST00000420008.2:c.1053C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1053C>T
  hgvsp: ENST00000483892.1:c.1053C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13030
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28642
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1263
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2615
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg522Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

7-148876553-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876553
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876553
    reference: chr 7
allele count: 2
allele frequency: 1.649022129876983e-5
allele num: 121284
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1076G>A
  hgvsp: ENSP00000338984.4:p.Arg359Gln
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1589G>A
  hgvsp: ENSP00000420418.1:p.Arg530Gln
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1604G>A
  hgvsp: ENSP00000439340.1:p.Arg535Gln
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1076G>A
  hgvsp: ENSP00000419391.1:p.Arg359Gln
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1076G>A
  hgvsp: ENSP00000416751.2:p.Arg359Gln
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1076G>A
  hgvsp: ENSP00000418564.1:p.Arg359Gln
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1076G>A
  hgvsp: ENSP00000389972.2:p.Arg359Gln
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13012
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2038
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2606
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1254
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg530Gln
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

7-148876556-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876556
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876556
    reference: chr 7
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1079G>A
  hgvsp: ENSP00000418564.1:p.Arg360Gln
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1592G>A
  hgvsp: ENSP00000420418.1:p.Arg531Gln
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1079G>A
  hgvsp: ENSP00000389972.2:p.Arg360Gln
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1607G>A
  hgvsp: ENSP00000439340.1:p.Arg536Gln
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1079G>A
  hgvsp: ENSP00000419391.1:p.Arg360Gln
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1079G>A
  hgvsp: ENSP00000338984.4:p.Arg360Gln
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1079G>A
  hgvsp: ENSP00000416751.2:p.Arg360Gln
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg531Gln
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD

7-148876578-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876578
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876578
    reference: chr 7
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1614C>T
  hgvsp: ENST00000475153.1:c.1614C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1101C>T
  hgvsp: ENST00000426851.2:c.1101C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1101C>T
  hgvsp: ENST00000335901.4:c.1101C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1101C>T
  hgvsp: ENST00000483892.1:c.1101C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1629C>T
  hgvsp: ENST00000540950.1:c.1629C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1101C>T
  hgvsp: ENST00000420008.2:c.1101C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1101C>T
  hgvsp: ENST00000491174.1:c.1101C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28715
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40309
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1260
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2616
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro538Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

7-148876581-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876581
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876581
    reference: chr 7
allele count: 15
allele frequency: 1.236318079915601e-4
allele num: 121328
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1104C>T
  hgvsp: ENST00000491174.1:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1617C>T
  hgvsp: ENST00000475153.1:c.1617C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1632C>T
  hgvsp: ENST00000540950.1:c.1632C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1104C>T
  hgvsp: ENST00000420008.2:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1104C>T
  hgvsp: ENST00000426851.2:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1104C>T
  hgvsp: ENST00000335901.4:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1104C>T
  hgvsp: ENST00000483892.1:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28722
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11965
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13002
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10333
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2614
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Phe539Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

7-148876589-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876589
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876589
    reference: chr 7
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1625C>T
  hgvsp: ENSP00000420418.1:p.Pro542Leu
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1112C>T
  hgvsp: ENSP00000419391.1:p.Pro371Leu
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1112C>T
  hgvsp: ENSP00000338984.4:p.Pro371Leu
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1640C>T
  hgvsp: ENSP00000439340.1:p.Pro547Leu
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1112C>T
  hgvsp: ENSP00000389972.2:p.Pro371Leu
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1112C>T
  hgvsp: ENSP00000416751.2:p.Pro371Leu
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1112C>T
  hgvsp: ENSP00000418564.1:p.Pro371Leu
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28745
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2031
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2615
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10342
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro542Leu
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum

7-148876593-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876593
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876593
    reference: chr 7
allele count: 3
allele frequency: 2.47239162683369e-5
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1116C>T
  hgvsp: ENST00000491174.1:c.1116C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1629C>T
  hgvsp: ENST00000475153.1:c.1629C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1116C>T
  hgvsp: ENST00000420008.2:c.1116C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1116C>T
  hgvsp: ENST00000426851.2:c.1116C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1116C>T
  hgvsp: ENST00000483892.1:c.1116C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1116C>T
  hgvsp: ENST00000335901.4:c.1116C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1644C>T
  hgvsp: ENST00000540950.1:c.1644C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28759
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40393
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10347
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
hgvs: p.His543His
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

7-148876604-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876604
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876604
    reference: chr 7
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1127G>C
  hgvsp: ENSP00000416751.2:p.Ser376Thr
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1655G>C
  hgvsp: ENSP00000439340.1:p.Ser552Thr
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1640G>C
  hgvsp: ENSP00000420418.1:p.Ser547Thr
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1127G>C
  hgvsp: ENSP00000389972.2:p.Ser376Thr
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1127G>C
  hgvsp: ENSP00000418564.1:p.Ser376Thr
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1127G>C
  hgvsp: ENSP00000419391.1:p.Ser376Thr
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1127G>C
  hgvsp: ENSP00000338984.4:p.Ser376Thr
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28791
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13030
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2027
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2748
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser547Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ

7-148876608-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876608
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876608
    reference: chr 7
allele count: 14
allele frequency: 1.153535586572846e-4
allele num: 121366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1131C>T
  hgvsp: ENST00000335901.4:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1131C>T
  hgvsp: ENST00000426851.2:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1644C>T
  hgvsp: ENST00000475153.1:c.1644C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1131C>T
  hgvsp: ENST00000420008.2:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1659C>T
  hgvsp: ENST00000540950.1:c.1659C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1131C>T
  hgvsp: ENST00000491174.1:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1131C>T
  hgvsp: ENST00000483892.1:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28790
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Phe548Phe
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

7-148876613-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876613
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876613
    reference: chr 7
allele count: 1
allele frequency: 8.239811473113496e-6
allele num: 121362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1136G>A
  hgvsp: ENSP00000338984.4:p.Arg379His
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1649G>A
  hgvsp: ENSP00000420418.1:p.Arg550His
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1136G>A
  hgvsp: ENSP00000416751.2:p.Arg379His
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1136G>A
  hgvsp: ENSP00000389972.2:p.Arg379His
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1136G>A
  hgvsp: ENSP00000418564.1:p.Arg379His
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1136G>A
  hgvsp: ENSP00000419391.1:p.Arg379His
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1664G>A
  hgvsp: ENSP00000439340.1:p.Arg555His
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2914
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28803
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11979
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2748
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10359
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2619
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40433
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg550His
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP

7-148876650-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876650
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876650
    reference: chr 7
allele count: 2
allele frequency: 1.647907980818351e-5
allele num: 121366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1173C>T
  hgvsp: ENST00000483892.1:c.1173C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1173C>T
  hgvsp: ENST00000420008.2:c.1173C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1701C>T
  hgvsp: ENST00000540950.1:c.1701C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1173C>T
  hgvsp: ENST00000426851.2:c.1173C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1173C>T
  hgvsp: ENST00000491174.1:c.1173C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1173C>T
  hgvsp: ENST00000335901.4:c.1173C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1686C>T
  hgvsp: ENST00000475153.1:c.1686C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 576
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40356
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1260
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr562Thr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

7-148876651-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876651
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876651
    reference: chr 7
allele count: 6
allele frequency: 4.943316635908252e-5
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1174G>A
  hgvsp: ENSP00000418564.1:p.Gly392Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1174G>A
  hgvsp: ENSP00000389972.2:p.Gly392Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1702G>A
  hgvsp: ENSP00000439340.1:p.Gly568Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1174G>A
  hgvsp: ENSP00000338984.4:p.Gly392Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1174G>A
  hgvsp: ENSP00000416751.2:p.Gly392Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1174G>A
  hgvsp: ENSP00000419391.1:p.Gly392Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1687G>A
  hgvsp: ENSP00000420418.1:p.Gly563Arg
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28803
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly563Arg
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

7-148876656-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876656
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876656
    reference: chr 7
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1707G>A
  hgvsp: ENST00000540950.1:c.1707G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1179G>A
  hgvsp: ENST00000420008.2:c.1179G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1179G>A
  hgvsp: ENST00000483892.1:c.1179G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1179G>A
  hgvsp: ENST00000491174.1:c.1179G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1692G>A
  hgvsp: ENST00000475153.1:c.1692G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1179G>A
  hgvsp: ENST00000335901.4:c.1179G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1179G>A
  hgvsp: ENST00000426851.2:c.1179G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28779
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11887
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2730
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1265
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu564Glu
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

7-148876657-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876657
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876657
    reference: chr 7
allele count: 2
allele frequency: 1.647772211969417e-5
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1693C>T
  hgvsp: ENSP00000420418.1:p.Arg565Trp
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1180C>T
  hgvsp: ENSP00000418564.1:p.Arg394Trp
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1180C>T
  hgvsp: ENSP00000419391.1:p.Arg394Trp
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1180C>T
  hgvsp: ENSP00000416751.2:p.Arg394Trp
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1180C>T
  hgvsp: ENSP00000338984.4:p.Arg394Trp
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1180C>T
  hgvsp: ENSP00000389972.2:p.Arg394Trp
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1708C>T
  hgvsp: ENSP00000439340.1:p.Arg570Trp
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11876
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28764
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2729
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40266
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2620
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg565Trp
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

7-148876658-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876658
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876658
    reference: chr 7
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1181G>A
  hgvsp: ENSP00000338984.4:p.Arg394Gln
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1181G>A
  hgvsp: ENSP00000416751.2:p.Arg394Gln
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1181G>A
  hgvsp: ENSP00000389972.2:p.Arg394Gln
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1694G>A
  hgvsp: ENSP00000420418.1:p.Arg565Gln
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1181G>A
  hgvsp: ENSP00000419391.1:p.Arg394Gln
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1181G>A
  hgvsp: ENSP00000418564.1:p.Arg394Gln
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1709G>A
  hgvsp: ENSP00000439340.1:p.Arg570Gln
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11879
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13056
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28765
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40289
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg565Gln
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: G
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

7-148876666-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876666
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876666
    reference: chr 7
allele count: 2
allele frequency: 1.647989452867502e-5
allele num: 121360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1189C>T
  hgvsp: ENSP00000389972.2:p.Pro397Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1189C>T
  hgvsp: ENSP00000338984.4:p.Pro397Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1702C>T
  hgvsp: ENSP00000420418.1:p.Pro568Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1189C>T
  hgvsp: ENSP00000418564.1:p.Pro397Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1189C>T
  hgvsp: ENSP00000419391.1:p.Pro397Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1189C>T
  hgvsp: ENSP00000416751.2:p.Pro397Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1717C>T
  hgvsp: ENSP00000439340.1:p.Pro573Ser
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2725
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro568Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/7-148876684-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876684
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876684
    reference: chr 7
allele count: 3
allele frequency: 2.481020195504391e-5
allele num: 120918
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1207A>C
  hgvsp: ENST00000335901.4:c.1207A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1207A>C
  hgvsp: ENST00000491174.1:c.1207A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1735A>C
  hgvsp: ENST00000540950.1:c.1735A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1720A>C
  hgvsp: ENST00000475153.1:c.1720A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1207A>C
  hgvsp: ENST00000483892.1:c.1207A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1207A>C
  hgvsp: ENST00000426851.2:c.1207A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1207A>C
  hgvsp: ENST00000420008.2:c.1207A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28039
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11520
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12666
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1183
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38773
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg574Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

7-148876687-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876687
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876687
    reference: chr 7
allele count: 43
allele frequency: 3.879115922417682e-4
allele num: 110850
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1210A>G
  hgvsp: ENSP00000416751.2:p.Ser404Gly
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1210A>G
  hgvsp: ENSP00000418564.1:p.Ser404Gly
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1723A>G
  hgvsp: ENSP00000420418.1:p.Ser575Gly
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1738A>G
  hgvsp: ENSP00000439340.1:p.Ser580Gly
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1210A>G
  hgvsp: ENSP00000419391.1:p.Ser404Gly
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1210A>G
  hgvsp: ENSP00000389972.2:p.Ser404Gly
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1210A>G
  hgvsp: ENSP00000338984.4:p.Ser404Gly
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12537
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27986
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2644
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11449
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4902
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2322
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9391
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 9.25e1
  variant carriers: 3
hgvs: p.Ser575Gly
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum

7-148876689-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876689
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876689
    reference: chr 7
allele count: 9
allele frequency: 7.468012015201553e-5
allele num: 120514
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1212C>G
  hgvsp: ENSP00000338984.4:p.Ser404Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1212C>G
  hgvsp: ENSP00000416751.2:p.Ser404Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1725C>G
  hgvsp: ENSP00000420418.1:p.Ser575Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1212C>G
  hgvsp: ENSP00000418564.1:p.Ser404Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1740C>G
  hgvsp: ENSP00000439340.1:p.Ser580Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1212C>G
  hgvsp: ENSP00000419391.1:p.Ser404Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1212C>G
  hgvsp: ENSP00000389972.2:p.Ser404Arg
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 11897
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29637
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13400
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1185
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2631
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1434
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39980
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser575Arg
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP

7-148876693-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876693
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876693
    reference: chr 7
allele count: 3
allele frequency: 2.473859550747106e-5
allele num: 121268
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1216C>T
  hgvsp: ENSP00000419391.1:p.Arg406Cys
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1216C>T
  hgvsp: ENSP00000389972.2:p.Arg406Cys
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1216C>T
  hgvsp: ENSP00000416751.2:p.Arg406Cys
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1744C>T
  hgvsp: ENSP00000439340.1:p.Arg582Cys
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1729C>T
  hgvsp: ENSP00000420418.1:p.Arg577Cys
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1216C>T
  hgvsp: ENSP00000338984.4:p.Arg406Cys
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1216C>T
  hgvsp: ENSP00000418564.1:p.Arg406Cys
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11957
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 40443
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg577Cys
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

7-148876694-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876694
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876694
    reference: chr 7
allele count: 2
allele frequency: 1.649375711293276e-5
allele num: 121258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1217G>A
  hgvsp: ENSP00000338984.4:p.Arg406His
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1217G>A
  hgvsp: ENSP00000416751.2:p.Arg406His
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1730G>A
  hgvsp: ENSP00000420418.1:p.Arg577His
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1217G>A
  hgvsp: ENSP00000419391.1:p.Arg406His
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1217G>A
  hgvsp: ENSP00000389972.2:p.Arg406His
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1745G>A
  hgvsp: ENSP00000439340.1:p.Arg582His
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1217G>A
  hgvsp: ENSP00000418564.1:p.Arg406His
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2681
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12013
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10459
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg577His
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

7-148876694-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876694
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876694
    reference: chr 7
allele count: 1
allele frequency: 8.246878556466378e-6
allele num: 121258
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1217G>C
  hgvsp: ENSP00000416751.2:p.Arg406Pro
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1730G>C
  hgvsp: ENSP00000420418.1:p.Arg577Pro
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1217G>C
  hgvsp: ENSP00000418564.1:p.Arg406Pro
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1217G>C
  hgvsp: ENSP00000389972.2:p.Arg406Pro
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1217G>C
  hgvsp: ENSP00000338984.4:p.Arg406Pro
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1217G>C
  hgvsp: ENSP00000419391.1:p.Arg406Pro
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1745G>C
  hgvsp: ENSP00000439340.1:p.Arg582Pro
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12013
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1494
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40461
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg577Pro
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

7-148876705-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876705
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876705
    reference: chr 7
allele count: 1
allele frequency: 8.24551856066228e-6
allele num: 121278
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1741A>G
  hgvsp: ENSP00000420418.1:p.Thr581Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1228A>G
  hgvsp: ENSP00000418564.1:p.Thr410Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1228A>G
  hgvsp: ENSP00000389972.2:p.Thr410Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1756A>G
  hgvsp: ENSP00000439340.1:p.Thr586Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1228A>G
  hgvsp: ENSP00000419391.1:p.Thr410Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1228A>G
  hgvsp: ENSP00000338984.4:p.Thr410Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1228A>G
  hgvsp: ENSP00000416751.2:p.Thr410Ala
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29859
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2562
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10472
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1230
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr581Ala
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD

7-148876708-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876708
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876708
    reference: chr 7
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1231C>G
  hgvsp: ENSP00000416751.2:p.Leu411Val
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1231C>G
  hgvsp: ENSP00000419391.1:p.Leu411Val
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1231C>G
  hgvsp: ENSP00000338984.4:p.Leu411Val
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1744C>G
  hgvsp: ENSP00000420418.1:p.Leu582Val
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1231C>G
  hgvsp: ENSP00000418564.1:p.Leu411Val
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1759C>G
  hgvsp: ENSP00000439340.1:p.Leu587Val
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1231C>G
  hgvsp: ENSP00000389972.2:p.Leu411Val
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29891
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2564
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10471
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1226
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu582Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

7-148876710-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876710
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876710
    reference: chr 7
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1233C>G
  hgvsp: ENST00000491174.1:c.1233C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1761C>G
  hgvsp: ENST00000540950.1:c.1761C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1233C>G
  hgvsp: ENST00000335901.4:c.1233C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1233C>G
  hgvsp: ENST00000426851.2:c.1233C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1746C>G
  hgvsp: ENST00000475153.1:c.1746C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1233C>G
  hgvsp: ENST00000483892.1:c.1233C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1233C>G
  hgvsp: ENST00000420008.2:c.1233C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12134
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13449
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2664
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2559
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10460
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu582Leu
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

7-148876723-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876723
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876723
    reference: chr 7
allele count: 1
allele frequency: 8.244974687927709e-6
allele num: 121286
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1774C>T
  hgvsp: ENSP00000439340.1:p.Arg592Cys
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1246C>T
  hgvsp: ENSP00000416751.2:p.Arg416Cys
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1759C>T
  hgvsp: ENSP00000420418.1:p.Arg587Cys
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1246C>T
  hgvsp: ENSP00000389972.2:p.Arg416Cys
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1246C>T
  hgvsp: ENSP00000338984.4:p.Arg416Cys
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1246C>T
  hgvsp: ENSP00000419391.1:p.Arg416Cys
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1246C>T
  hgvsp: ENSP00000418564.1:p.Arg416Cys
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2570
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1477
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10475
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg587Cys
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

7-148876724-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876724
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876724
    reference: chr 7
allele count: 2
allele frequency: 1.648967746190884e-5
allele num: 121288
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1247G>A
  hgvsp: ENSP00000338984.4:p.Arg416His
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1247G>A
  hgvsp: ENSP00000389972.2:p.Arg416His
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1760G>A
  hgvsp: ENSP00000420418.1:p.Arg587His
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1247G>A
  hgvsp: ENSP00000418564.1:p.Arg416His
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1247G>A
  hgvsp: ENSP00000416751.2:p.Arg416His
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1247G>A
  hgvsp: ENSP00000419391.1:p.Arg416His
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1775G>A
  hgvsp: ENSP00000439340.1:p.Arg592His
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12153
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30031
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2571
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40803
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg587His
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

7-148876734-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876734
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876734
    reference: chr 7
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1770C>G
  hgvsp: ENSP00000420418.1:p.His590Gln
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1257C>G
  hgvsp: ENSP00000416751.2:p.His419Gln
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1257C>G
  hgvsp: ENSP00000389972.2:p.His419Gln
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1257C>G
  hgvsp: ENSP00000419391.1:p.His419Gln
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1785C>G
  hgvsp: ENSP00000439340.1:p.His595Gln
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1257C>G
  hgvsp: ENSP00000418564.1:p.His419Gln
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1257C>G
  hgvsp: ENSP00000338984.4:p.His419Gln
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13416
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1474
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1226
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10470
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.His590Gln
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum

7-148876735-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876735
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876735
    reference: chr 7
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1258A>G
  hgvsp: ENSP00000418564.1:p.Asn420Asp
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1258A>G
  hgvsp: ENSP00000419391.1:p.Asn420Asp
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1771A>G
  hgvsp: ENSP00000420418.1:p.Asn591Asp
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1786A>G
  hgvsp: ENSP00000439340.1:p.Asn596Asp
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1258A>G
  hgvsp: ENSP00000338984.4:p.Asn420Asp
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1258A>G
  hgvsp: ENSP00000389972.2:p.Asn420Asp
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1258A>G
  hgvsp: ENSP00000416751.2:p.Asn420Asp
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12193
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30060
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10472
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2665
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2570
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn591Asp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

7-148876736-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876736
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876736
    reference: chr 7
allele count: 10
allele frequency: 8.244566830458728e-5
allele num: 121292
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1259A>G
  hgvsp: ENSP00000389972.2:p.Asn420Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1259A>G
  hgvsp: ENSP00000418564.1:p.Asn420Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1259A>G
  hgvsp: ENSP00000416751.2:p.Asn420Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1259A>G
  hgvsp: ENSP00000419391.1:p.Asn420Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1787A>G
  hgvsp: ENSP00000439340.1:p.Asn596Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1772A>G
  hgvsp: ENSP00000420418.1:p.Asn591Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1259A>G
  hgvsp: ENSP00000338984.4:p.Asn420Ser
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30058
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12197
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1228
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1477
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asn591Ser
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

7-148876742-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876742
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876742
    reference: chr 7
allele count: 2
allele frequency: 1.649022129876983e-5
allele num: 121284
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1265G>A
  hgvsp: ENSP00000389972.2:p.Gly422Asp
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1265G>A
  hgvsp: ENSP00000338984.4:p.Gly422Asp
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1265G>A
  hgvsp: ENSP00000419391.1:p.Gly422Asp
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1778G>A
  hgvsp: ENSP00000420418.1:p.Gly593Asp
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1265G>A
  hgvsp: ENSP00000418564.1:p.Gly422Asp
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1793G>A
  hgvsp: ENSP00000439340.1:p.Gly598Asp
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1265G>A
  hgvsp: ENSP00000416751.2:p.Gly422Asp
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2642
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10482
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1225
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1467
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Gly593Asp
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

7-148876745-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876745
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876745
    reference: chr 7
allele count: 5
allele frequency: 4.122623307663132e-5
allele num: 121282
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1268G>C
  hgvsp: ENSP00000389972.2:p.Cys423Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1796G>C
  hgvsp: ENSP00000439340.1:p.Cys599Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1268G>C
  hgvsp: ENSP00000419391.1:p.Cys423Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1781G>C
  hgvsp: ENSP00000420418.1:p.Cys594Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1268G>C
  hgvsp: ENSP00000416751.2:p.Cys423Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1268G>C
  hgvsp: ENSP00000338984.4:p.Cys423Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1268G>C
  hgvsp: ENSP00000418564.1:p.Cys423Ser
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12209
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10486
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1223
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Cys594Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

7-148876746-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876746
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876746
    reference: chr 7
allele count: 2
allele frequency: 1.649212501030758e-5
allele num: 121270
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1782T>C
  hgvsp: ENST00000475153.1:c.1782T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1797T>C
  hgvsp: ENST00000540950.1:c.1797T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1269T>C
  hgvsp: ENST00000335901.4:c.1269T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1269T>C
  hgvsp: ENST00000420008.2:c.1269T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1269T>C
  hgvsp: ENST00000483892.1:c.1269T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1269T>C
  hgvsp: ENST00000426851.2:c.1269T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1269T>C
  hgvsp: ENST00000491174.1:c.1269T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30072
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2647
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1221
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2663
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Cys594Cys
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD

7-148876751-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876751
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876751
    reference: chr 7
allele count: 1
allele frequency: 8.246878556466378e-6
allele num: 121258
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1787G>T
  hgvsp: ENSP00000420418.1:p.Gly596Val
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1274G>T
  hgvsp: ENSP00000419391.1:p.Gly425Val
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1274G>T
  hgvsp: ENSP00000338984.4:p.Gly425Val
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1274G>T
  hgvsp: ENSP00000416751.2:p.Gly425Val
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1274G>T
  hgvsp: ENSP00000389972.2:p.Gly425Val
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1802G>T
  hgvsp: ENSP00000439340.1:p.Gly601Val
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1274G>T
  hgvsp: ENSP00000418564.1:p.Gly425Val
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2658
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2557
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly596Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

7-148876768-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876768
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876768
    reference: chr 7
allele count: 1
allele frequency: 8.248102936324645e-6
allele num: 121240
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1291G>C
  hgvsp: ENSP00000389972.2:p.Gly431Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1291G>C
  hgvsp: ENSP00000416751.2:p.Gly431Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1291G>C
  hgvsp: ENSP00000338984.4:p.Gly431Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1819G>C
  hgvsp: ENSP00000439340.1:p.Gly607Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1804G>C
  hgvsp: ENSP00000420418.1:p.Gly602Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1291G>C
  hgvsp: ENSP00000418564.1:p.Gly431Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1291G>C
  hgvsp: ENSP00000419391.1:p.Gly431Arg
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13346
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1209
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2550
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10420
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1467
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly602Arg
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

7-148876777-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876777
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876777
    reference: chr 7
allele count: 2
allele frequency: 1.650273945474949e-5
allele num: 121192
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1813C>T
  hgvsp: ENSP00000420418.1:p.Pro605Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1300C>T
  hgvsp: ENSP00000338984.4:p.Pro434Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1300C>T
  hgvsp: ENSP00000418564.1:p.Pro434Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1300C>T
  hgvsp: ENSP00000389972.2:p.Pro434Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1300C>T
  hgvsp: ENSP00000416751.2:p.Pro434Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1300C>T
  hgvsp: ENSP00000419391.1:p.Pro434Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1828C>T
  hgvsp: ENSP00000439340.1:p.Pro610Ser
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13238
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1191
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro605Ser
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

7-148876783-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876783
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876783
    reference: chr 7
allele count: 54
allele frequency: 4.457873099212442e-4
allele num: 121134
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1306C>G
  hgvsp: ENSP00000416751.2:p.Pro436Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1306C>G
  hgvsp: ENSP00000389972.2:p.Pro436Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1819C>G
  hgvsp: ENSP00000420418.1:p.Pro607Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1306C>G
  hgvsp: ENSP00000419391.1:p.Pro436Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1306C>G
  hgvsp: ENSP00000338984.4:p.Pro436Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1834C>G
  hgvsp: ENSP00000439340.1:p.Pro612Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1306C>G
  hgvsp: ENSP00000418564.1:p.Pro436Ala
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13164
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12342
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 29934
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2513
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1456
  bin: 9.75e1
  variant carriers: 53
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro607Ala
num of homozygotes: 1
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

7-148876783-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876783
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876783
    reference: chr 7
allele count: 4
allele frequency: 3.302128221638846e-5
allele num: 121134
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1306C>T
  hgvsp: ENSP00000418564.1:p.Pro436Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1306C>T
  hgvsp: ENSP00000338984.4:p.Pro436Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1834C>T
  hgvsp: ENSP00000439340.1:p.Pro612Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1819C>T
  hgvsp: ENSP00000420418.1:p.Pro607Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1306C>T
  hgvsp: ENSP00000389972.2:p.Pro436Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1306C>T
  hgvsp: ENSP00000416751.2:p.Pro436Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1306C>T
  hgvsp: ENSP00000419391.1:p.Pro436Ser
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13164
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29934
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12342
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10255
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2513
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro607Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

7-148876786-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876786
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876786
    reference: chr 7
allele count: 2
allele frequency: 1.650982334489021e-5
allele num: 121140
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1837C>G
  hgvsp: ENSP00000439340.1:p.Pro613Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1822C>G
  hgvsp: ENSP00000420418.1:p.Pro608Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1309C>G
  hgvsp: ENSP00000338984.4:p.Pro437Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1309C>G
  hgvsp: ENSP00000389972.2:p.Pro437Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1309C>G
  hgvsp: ENSP00000419391.1:p.Pro437Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1309C>G
  hgvsp: ENSP00000416751.2:p.Pro437Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1309C>G
  hgvsp: ENSP00000418564.1:p.Pro437Ala
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29984
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12386
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40831
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2511
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1180
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Pro608Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

7-148876799-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876799
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876799
    reference: chr 7
allele count: 2
allele frequency: 1.655601728448204e-5
allele num: 120802
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1835T>A
  hgvsp: ENSP00000420418.1:p.Ile612Lys
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1322T>A
  hgvsp: ENSP00000419391.1:p.Ile441Lys
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1322T>A
  hgvsp: ENSP00000338984.4:p.Ile441Lys
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1850T>A
  hgvsp: ENSP00000439340.1:p.Ile617Lys
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1322T>A
  hgvsp: ENSP00000389972.2:p.Ile441Lys
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1322T>A
  hgvsp: ENSP00000418564.1:p.Ile441Lys
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1322T>A
  hgvsp: ENSP00000416751.2:p.Ile441Lys
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29839
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12934
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10112
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile612Lys
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

7-148876803-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876803
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876803
    reference: chr 7
allele count: 1
allele frequency: 8.285004142502071e-6
allele num: 120700
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1326T>C
  hgvsp: ENST00000426851.2:c.1326T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1839T>C
  hgvsp: ENST00000475153.1:c.1839T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1326T>C
  hgvsp: ENST00000335901.4:c.1326T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1854T>C
  hgvsp: ENST00000540950.1:c.1854T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1326T>C
  hgvsp: ENST00000483892.1:c.1326T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1326T>C
  hgvsp: ENST00000420008.2:c.1326T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1326T>C
  hgvsp: ENST00000491174.1:c.1326T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29785
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12477
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12895
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10089
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40634
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr613Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

7-148876808-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876808
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876808
    reference: chr 7
allele count: 2
allele frequency: 1.660826094899603e-5
allele num: 120422
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1331T>G
  hgvsp: ENSP00000389972.2:p.Leu444Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1331T>G
  hgvsp: ENSP00000338984.4:p.Leu444Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1859T>G
  hgvsp: ENSP00000439340.1:p.Leu620Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1331T>G
  hgvsp: ENSP00000419391.1:p.Leu444Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1331T>G
  hgvsp: ENSP00000418564.1:p.Leu444Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1844T>G
  hgvsp: ENSP00000420418.1:p.Leu615Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1331T>G
  hgvsp: ENSP00000416751.2:p.Leu444Arg
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12825
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12370
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40427
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1139
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1385
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Leu615Arg
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/7-148876814-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876814
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876814
    reference: chr 7
allele count: 1
allele frequency: 8.332638946754437e-6
allele num: 120010
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1337C>A
  hgvsp: ENSP00000419391.1:p.Thr446Asn
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1865C>A
  hgvsp: ENSP00000439340.1:p.Thr622Asn
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1337C>A
  hgvsp: ENSP00000338984.4:p.Thr446Asn
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1337C>A
  hgvsp: ENSP00000416751.2:p.Thr446Asn
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1850C>A
  hgvsp: ENSP00000420418.1:p.Thr617Asn
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1337C>A
  hgvsp: ENSP00000418564.1:p.Thr446Asn
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1337C>A
  hgvsp: ENSP00000389972.2:p.Thr446Asn
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29460
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2526
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1169
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40126
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr617Asn
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS

7-148876818-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876818
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876818
    reference: chr 7
allele count: 2
allele frequency: 1.672548462091689e-5
allele num: 119578
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1869T>C
  hgvsp: ENST00000540950.1:c.1869T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1341T>C
  hgvsp: ENST00000426851.2:c.1341T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1341T>C
  hgvsp: ENST00000335901.4:c.1341T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1341T>C
  hgvsp: ENST00000420008.2:c.1341T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1854T>C
  hgvsp: ENST00000475153.1:c.1854T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1341T>C
  hgvsp: ENST00000491174.1:c.1341T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1341T>C
  hgvsp: ENST00000483892.1:c.1341T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29246
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12720
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12015
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39602
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1381
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser618Ser
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

7-148876841-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876841
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876841
    reference: chr 7
allele count: 88
allele frequency: 7.49242243639955e-4
allele num: 117452
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1364G>A
  hgvsp: ENSP00000389972.2:p.Gly455Asp
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1364G>A
  hgvsp: ENSP00000416751.2:p.Gly455Asp
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1364G>A
  hgvsp: ENSP00000419391.1:p.Gly455Asp
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1364G>A
  hgvsp: ENSP00000338984.4:p.Gly455Asp
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1877G>A
  hgvsp: ENSP00000420418.1:p.Gly626Asp
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1364G>A
  hgvsp: ENSP00000418564.1:p.Gly455Asp
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1892G>A
  hgvsp: ENSP00000439340.1:p.Gly631Asp
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 10934
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12502
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28510
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2334
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3274
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1103
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly626Asp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

7-148876841-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876841
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876841
    reference: chr 7
allele count: 1
allele frequency: 8.514116404999489e-6
allele num: 117452
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1892G>T
  hgvsp: ENSP00000439340.1:p.Gly631Val
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1364G>T
  hgvsp: ENSP00000338984.4:p.Gly455Val
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1364G>T
  hgvsp: ENSP00000389972.2:p.Gly455Val
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1364G>T
  hgvsp: ENSP00000416751.2:p.Gly455Val
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1364G>T
  hgvsp: ENSP00000418564.1:p.Gly455Val
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1877G>T
  hgvsp: ENSP00000420418.1:p.Gly626Val
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1364G>T
  hgvsp: ENSP00000419391.1:p.Gly455Val
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10934
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9734
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1103
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2334
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly626Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: African
reference allele: G
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

7-148876842-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876842
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876842
    reference: chr 7
allele count: 1
allele frequency: 8.522533578782301e-6
allele num: 117336
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1365T>C
  hgvsp: ENST00000335901.4:c.1365T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1893T>C
  hgvsp: ENST00000540950.1:c.1893T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1365T>C
  hgvsp: ENST00000483892.1:c.1365T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1365T>C
  hgvsp: ENST00000426851.2:c.1365T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1365T>C
  hgvsp: ENST00000491174.1:c.1365T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1878T>C
  hgvsp: ENST00000475153.1:c.1878T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1365T>C
  hgvsp: ENST00000420008.2:c.1365T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12513
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2334
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38050
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3331
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9748
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gly626Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

7-148876849-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876849
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876849
    reference: chr 7
allele count: 1
allele frequency: 8.566924816667809e-6
allele num: 116728
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1900A>G
  hgvsp: ENSP00000439340.1:p.Thr634Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1372A>G
  hgvsp: ENSP00000389972.2:p.Thr458Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1372A>G
  hgvsp: ENSP00000419391.1:p.Thr458Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1372A>G
  hgvsp: ENSP00000416751.2:p.Thr458Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1885A>G
  hgvsp: ENSP00000420418.1:p.Thr629Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1372A>G
  hgvsp: ENSP00000338984.4:p.Thr458Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1372A>G
  hgvsp: ENSP00000418564.1:p.Thr458Ala
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3773
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37657
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1099
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr629Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

7-148876865-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876865
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876865
    reference: chr 7
allele count: 1
allele frequency: 8.687493484379887e-6
allele num: 115108
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1388G>T
  hgvsp: ENSP00000389972.2:p.Gly463Val
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1901G>T
  hgvsp: ENSP00000420418.1:p.Gly634Val
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1388G>T
  hgvsp: ENSP00000418564.1:p.Gly463Val
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1916G>T
  hgvsp: ENSP00000439340.1:p.Gly639Val
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1388G>T
  hgvsp: ENSP00000419391.1:p.Gly463Val
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1388G>T
  hgvsp: ENSP00000416751.2:p.Gly463Val
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1388G>T
  hgvsp: ENSP00000338984.4:p.Gly463Val
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2586
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2402
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4554
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36962
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gly634Val
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/7-148876868-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876868
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876868
    reference: chr 7
allele count: 1
allele frequency: 8.733319360022357e-6
allele num: 114504
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1391A>C
  hgvsp: ENSP00000389972.2:p.Glu464Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1919A>C
  hgvsp: ENSP00000439340.1:p.Glu640Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1391A>C
  hgvsp: ENSP00000416751.2:p.Glu464Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1904A>C
  hgvsp: ENSP00000420418.1:p.Glu635Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1391A>C
  hgvsp: ENSP00000338984.4:p.Glu464Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1391A>C
  hgvsp: ENSP00000418564.1:p.Glu464Ala
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1391A>C
  hgvsp: ENSP00000419391.1:p.Glu464Ala
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2752
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9643
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28106
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4601
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu635Ala
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

7-148876871-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876871
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876871
    reference: chr 7
allele count: 1
allele frequency: 8.800802633200148e-6
allele num: 113626
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1394G>A
  hgvsp: ENSP00000416751.2:p.Gly465Glu
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1394G>A
  hgvsp: ENSP00000419391.1:p.Gly465Glu
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1394G>A
  hgvsp: ENSP00000418564.1:p.Gly465Glu
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1907G>A
  hgvsp: ENSP00000420418.1:p.Gly636Glu
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1922G>A
  hgvsp: ENSP00000439340.1:p.Gly641Glu
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1394G>A
  hgvsp: ENSP00000338984.4:p.Gly465Glu
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1394G>A
  hgvsp: ENSP00000389972.2:p.Gly465Glu
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9527
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4466
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 958
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36314
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gly636Glu
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

7-148876875-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876875
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876875
    reference: chr 7
allele count: 5
allele frequency: 4.419850432261373e-5
allele num: 113126
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1926T>C
  hgvsp: ENST00000540950.1:c.1926T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1398T>C
  hgvsp: ENST00000335901.4:c.1398T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1398T>C
  hgvsp: ENST00000483892.1:c.1398T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1398T>C
  hgvsp: ENST00000491174.1:c.1398T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1911T>C
  hgvsp: ENST00000475153.1:c.1911T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1398T>C
  hgvsp: ENST00000426851.2:c.1398T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1398T>C
  hgvsp: ENST00000420008.2:c.1398T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27825
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12300
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4503
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1132
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2266
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser637Ser
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

7-148876879-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876879
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876879
    reference: chr 7
allele count: 1
allele frequency: 8.891101785333239e-6
allele num: 112472
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1402G>C
  hgvsp: ENSP00000418564.1:p.Gly468Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1402G>C
  hgvsp: ENSP00000416751.2:p.Gly468Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1402G>C
  hgvsp: ENSP00000389972.2:p.Gly468Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1915G>C
  hgvsp: ENSP00000420418.1:p.Gly639Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1930G>C
  hgvsp: ENSP00000439340.1:p.Gly644Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1402G>C
  hgvsp: ENSP00000338984.4:p.Gly468Arg
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1402G>C
  hgvsp: ENSP00000419391.1:p.Gly468Arg
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27661
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2442
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4407
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2248
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9451
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35956
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly639Arg
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

7-148876889-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876889
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876889
    reference: chr 7
allele count: 1
allele frequency: 9.043226623259178e-6
allele num: 110580
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1412T>C
  hgvsp: ENSP00000389972.2:p.Leu471Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1412T>C
  hgvsp: ENSP00000338984.4:p.Leu471Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1940T>C
  hgvsp: ENSP00000439340.1:p.Leu647Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1925T>C
  hgvsp: ENSP00000420418.1:p.Leu642Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1412T>C
  hgvsp: ENSP00000418564.1:p.Leu471Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1412T>C
  hgvsp: ENSP00000419391.1:p.Leu471Ser
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1412T>C
  hgvsp: ENSP00000416751.2:p.Leu471Ser
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9429
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27103
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11958
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1030
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4329
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35330
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu642Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

7-148876890-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876890
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876890
    reference: chr 7
allele count: 1
allele frequency: 9.055182280819313e-6
allele num: 110434
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.1413G>A
  hgvsp: ENST00000335901.4:c.1413G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.1941G>A
  hgvsp: ENST00000540950.1:c.1941G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.1413G>A
  hgvsp: ENST00000491174.1:c.1413G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.1413G>A
  hgvsp: ENST00000483892.1:c.1413G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.1926G>A
  hgvsp: ENST00000475153.1:c.1926G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.1413G>A
  hgvsp: ENST00000426851.2:c.1413G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.1413G>A
  hgvsp: ENST00000420008.2:c.1413G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2503
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2162
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2156
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4324
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu642Leu
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP

7-148876899-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876899
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876899
    reference: chr 7
allele count: 2
allele frequency: 1.835401218706409e-5
allele num: 108968
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.*6A>G
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.*6A>G
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.*6A>G
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.*6A>G
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.*6A>G
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.*6A>G
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.*6A>G
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11592
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26181
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4487
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1267
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

7-148876928-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876928
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876928
    reference: chr 7
allele count: 1
allele frequency: 9.58552202752962e-6
allele num: 104324
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.*35T>C
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.*35T>C
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.*35T>C
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.*35T>C
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.*35T>C
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.*35T>C
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.*35T>C
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12093
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12492
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4050
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5594
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6234
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12738
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3833
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 562
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6551
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1275
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1700
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3790
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1905
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16106
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

7-148876929-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876929
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876929
    reference: chr 7
allele count: 1
allele frequency: 9.688232672595865e-6
allele num: 103218
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.*36C>G
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.*36C>G
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.*36C>G
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.*36C>G
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.*36C>G
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.*36C>G
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.*36C>G
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3852
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6668
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4039
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9972
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15971
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2926
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3626
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7729
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1011
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1186
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6788
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1239
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP

7-148876933-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876933
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876933
    reference: chr 7
allele count: 1
allele frequency: 9.706476160894549e-6
allele num: 103024
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.*40G>A
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.*40G>A
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.*40G>A
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.*40G>A
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.*40G>A
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.*40G>A
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.*40G>A
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3956
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4092
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15853
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9866
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7134
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12460
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3010
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2865
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2715
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 982
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 747
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7262
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4001
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 813
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

7-148876944-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148876944
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148876944
    reference: chr 7
allele count: 1
allele frequency: 9.982032341784787e-6
allele num: 100180
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000389972
  ensembl transcript: ENST00000426851
  gene symbol: ZNF398
  hgvsc: ENST00000426851.2:c.*51A>G
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000416751
  ensembl transcript: ENST00000420008
  gene symbol: ZNF398
  hgvsc: ENST00000420008.2:c.*51A>G
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000420418
  ensembl transcript: ENST00000475153
  gene symbol: ZNF398
  hgvsc: ENST00000475153.1:c.*51A>G
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000418564
  ensembl transcript: ENST00000483892
  gene symbol: ZNF398
  hgvsc: ENST00000483892.1:c.*51A>G
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000419391
  ensembl transcript: ENST00000491174
  gene symbol: ZNF398
  hgvsc: ENST00000491174.1:c.*51A>G
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000338984
  ensembl transcript: ENST00000335901
  gene symbol: ZNF398
  hgvsc: ENST00000335901.4:c.*51A>G
  variant of: http://identifiers.org/hgnc/18373
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197024
  ensembl protein: ENSP00000439340
  ensembl transcript: ENST00000540950
  gene symbol: ZNF398
  hgvsc: ENST00000540950.1:c.*51A>G
  variant of: http://identifiers.org/hgnc/18373
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11483
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16037
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
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genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
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genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4090
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
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  bin: 7.25e1
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genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2286
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1257
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

7-148892631-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148892631
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148892631
    reference: chr 7
allele count: 1
allele frequency: 1.036677655449815e-5
allele num: 96462
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170265
  ensembl protein: ENSP00000262085
  ensembl transcript: ENST00000262085
  gene symbol: ZNF282
  hgvsc: ENST00000262085.3:c.-51A>G
  variant of: http://identifiers.org/hgnc/13076
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5814
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1754
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7248
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 13870
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9716
  num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

7-148892634-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148892634
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148892634
    reference: chr 7
allele count: 3
allele frequency: 3.118243805088974e-5
allele num: 96208
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170265
  ensembl protein: ENSP00000262085
  ensembl transcript: ENST00000262085
  gene symbol: ZNF282
  hgvsc: ENST00000262085.3:c.-48C>T
  variant of: http://identifiers.org/hgnc/13076
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11073
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 1.882459244757351e-5
  allele num: 53122
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 2
  allele frequency: 2.060156571899464e-4
  allele num: 9708
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4232
  num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-148892635-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148892635
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148892635
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 96186
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170265
  ensembl protein: ENSP00000262085
  ensembl transcript: ENST00000262085
  gene symbol: ZNF282
  hgvsc: ENST00000262085.3:c.-47G>A
  variant of: http://identifiers.org/hgnc/13076
canonical: true
consequence: 5' UTR
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7204
  num of homozygotes: 0
population: African
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  allele count: 0
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  allele num: 7416
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 13848
  num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

7-148892635-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148892635
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148892635
    reference: chr 7
allele count: 4
allele frequency: 4.158609361029672e-5
allele num: 96186
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170265
  ensembl protein: ENSP00000262085
  ensembl transcript: ENST00000262085
  gene symbol: ZNF282
  hgvsc: ENST00000262085.3:c.-47G>C
  variant of: http://identifiers.org/hgnc/13076
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11707
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 5173
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7204
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4214
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7416
  num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP

7-148892636-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148892636
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148892636
    reference: chr 7
allele count: 1
allele frequency: 1.036806635562468e-5
allele num: 96450
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170265
  ensembl protein: ENSP00000262085
  ensembl transcript: ENST00000262085
  gene symbol: ZNF282
  hgvsc: ENST00000262085.3:c.-46T>C
  variant of: http://identifiers.org/hgnc/13076
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5933
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11765
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12318
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15349
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10409
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2294
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16317
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5709
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 853
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 10415
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 3341
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2551
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 30
  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 25
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genotype quality: GenotypeQuality
  all individuals: 2623
  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 3052
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4250
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9724
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 1.877511171191468e-5
  allele num: 53262
  num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

7-148892638-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148892638
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148892637
    reference: chr 7
allele count: 6
allele frequency: 6.228589224540641e-5
allele num: 96330
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170265
  ensembl protein: ENSP00000262085
  ensembl transcript: ENST00000262085
  gene symbol: ZNF282
  hgvsc: ENST00000262085.3:c.-42delT
  variant of: http://identifiers.org/hgnc/13076
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6004
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10620
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15253
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13478
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1736
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2952
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5701
  bin: 3.25e1
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genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3313
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1420
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10485
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1486
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6139
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 7.75e1
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genotype quality: GenotypeQuality
  all individuals: 2054
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 742
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2580
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genotype quality: GenotypeQuality
  all individuals: 17201
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 2
  allele frequency: 3.759822536376283e-5
  allele num: 53194
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 4
  allele frequency: 4.117768169652048e-4
  allele num: 9714
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7434
  num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: CT
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

7-148892644-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148892644
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148892644
    reference: chr 7
allele count: 1
allele frequency: 1.034404286571363e-5
allele num: 96674
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170265
  ensembl protein: ENSP00000262085
  ensembl transcript: ENST00000262085
  gene symbol: ZNF282
  hgvsc: ENST00000262085.3:c.-38C>T
  variant of: http://identifiers.org/hgnc/13076
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170265
  ensembl protein: ENSP00000418840
  ensembl transcript: ENST00000479907
  gene symbol: ZNF282
  hgvsc: ENST00000479907.1:c.-38C>T
  variant of: http://identifiers.org/hgnc/13076
canonical: true
consequence: 5' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14229
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6552
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  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 1405
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 175
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genotype quality: GenotypeQuality
  all individuals: 27
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 26
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3203
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 498
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  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7432
  num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ

7-148892659-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148892659
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148892659
    reference: chr 7
allele count: 8
allele frequency: 8.057206163762716e-5
allele num: 99290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170265
  ensembl protein: ENSP00000418840
  ensembl transcript: ENST00000479907
  gene symbol: ZNF282
  hgvsc: ENST00000479907.1:c.-23G>A
  variant of: http://identifiers.org/hgnc/13076
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170265
  ensembl protein: ENSP00000262085
  ensembl transcript: ENST00000262085
  gene symbol: ZNF282
  hgvsc: ENST00000262085.3:c.-23G>A
  variant of: http://identifiers.org/hgnc/13076
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9669
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7732
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  variant carriers: 2
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 11119
  bin: 2.25e1
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genotype quality: GenotypeQuality
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  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 483
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 317
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4450
  num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

7-148892661-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148892661
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148892661
    reference: chr 7
allele count: 1
allele frequency: 1.004157210852931e-5
allele num: 99586
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170265
  ensembl protein: ENSP00000262085
  ensembl transcript: ENST00000262085
  gene symbol: ZNF282
  hgvsc: ENST00000262085.3:c.-21G>A
  variant of: http://identifiers.org/hgnc/13076
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170265
  ensembl protein: ENSP00000418840
  ensembl transcript: ENST00000479907
  gene symbol: ZNF282
  hgvsc: ENST00000479907.1:c.-21G>A
  variant of: http://identifiers.org/hgnc/13076
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29009
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9579
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1104
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2533
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1965
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35069
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3354
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11039
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1545
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7568
  num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

7-148892663-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148892663
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 148892663
    reference: chr 7
allele count: 2
allele frequency: 2.001000500250125e-5
allele num: 99950
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170265
  ensembl protein: ENSP00000262085
  ensembl transcript: ENST00000262085
  gene symbol: ZNF282
  hgvsc: ENST00000262085.3:c.-19G>A
  variant of: http://identifiers.org/hgnc/13076
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170265
  ensembl protein: ENSP00000418840
  ensembl transcript: ENST00000479907
  gene symbol: ZNF282
  hgvsc: ENST00000479907.1:c.-19G>A
  variant of: http://identifiers.org/hgnc/13076
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 2698
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2045
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 76
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 70
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1265
bin: 8.25e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66640
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.23e1

MQ
type: SiteQuality
SIO_000300: 5.921e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.655e0

VQSLOD
type: SiteQuality
SIO_000300: 6.06e-1

DP
type: SiteQuality
SIO_000300: 1.765361e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.58e-1

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40059
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 62
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1266
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10305
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2699
bin: 7.25e1
variant carriers: 0

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

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

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

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

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

African
type: Population
allele count: 2
allele frequency: 1.925298421255295e-4
allele num: 10388
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.32e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.313e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.63e-1

FS
type: SiteQuality
SIO_000300: 4.906e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.65e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.43e0

DP
type: SiteQuality
SIO_000300: 1.766207e6

QD
type: SiteQuality
SIO_000300: 1.453e1

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

GenotypeQuality
all individuals: 10322
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2711
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2041
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2626
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 2.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500285054160291e-5
allele num: 66654
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.298e0

QD
type: SiteQuality
SIO_000300: 1.262e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e-1

DP
type: SiteQuality
SIO_000300: 1.767174e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.63e0

MQRankSum
type: SiteQuality
SIO_000300: -3.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.3e-1

GenotypeQuality
all individuals: 10316
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2039
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2718
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40226
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 2.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

FS
type: SiteQuality
SIO_000300: 1.199e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.31e-1

DP
type: SiteQuality
SIO_000300: 1.767473e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.534e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.04e0

MQRankSum
type: SiteQuality
SIO_000300: -1.92e-1

QD
type: SiteQuality
SIO_000300: 1.23e1

GenotypeQuality
all individuals: 10237
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2705
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 201
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39740
bin: 6.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000660145231951e-5
allele num: 66652
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

QD
type: SiteQuality
SIO_000300: 1.15e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 2.751e0

VQSLOD
type: SiteQuality
SIO_000300: -2.366e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.94e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.69e0

DP
type: SiteQuality
SIO_000300: 1.766555e6

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2611
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39838
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2036
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2711
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10264
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1254
bin: 8.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500060002400096e-5
allele num: 66664
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.765482e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.7e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

MQRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.22e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.59e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.585e1

GenotypeQuality
all individuals: 2038
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 104
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10333
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2738
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 38
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66672
num of homozygotes: 0

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

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.413e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
SIO_000300: 8.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.08e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.69e-1

DP
type: SiteQuality
SIO_000300: 1.768064e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.3e-1

FS
type: SiteQuality
SIO_000300: 3.053e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.4e-2

GenotypeQuality
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bin: 9.75e1
variant carriers: 15

GenotypeQuality
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bin: 8.25e1
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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 568
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variant carriers: 0

GenotypeQuality
all individuals: 2738
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 15
allele frequency: 1.443140273234558e-3
allele num: 10394
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.42e-1

DP
type: SiteQuality
SIO_000300: 1.769085e6

VQSLOD
type: SiteQuality
SIO_000300: 2.65e0

QD
type: SiteQuality
SIO_000300: 1.266e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.977e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.608e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.49e-1

GenotypeQuality
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bin: 1.25e1
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: 0

GenotypeQuality
all individuals: 0
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GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499655079331754e-5
allele num: 66682
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

FS
type: SiteQuality
SIO_000300: 5.31e-1

QD
type: SiteQuality
SIO_000300: 1.39e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.332e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e0

DP
type: SiteQuality
SIO_000300: 1.768928e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e0

VQSLOD
type: SiteQuality
SIO_000300: 2.93e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.35e-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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variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 3
allele frequency: 3.467406380027739e-4
allele num: 8652
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 2.504e0

DP
type: SiteQuality
SIO_000300: 1.769306e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.8e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

MQRankSum
type: SiteQuality
SIO_000300: 2.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

QD
type: SiteQuality
SIO_000300: 1.597e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.776e0

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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bin: 4.25e1
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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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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499430216517723e-5
allele num: 66692
num of homozygotes: 0

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

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
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VQSLOD
type: SiteQuality
SIO_000300: -2.103e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.49e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.769506e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.56e-1

QD
type: SiteQuality
SIO_000300: 1.4e1

FS
type: SiteQuality
SIO_000300: 1.3981e1

MQ
type: SiteQuality
SIO_000300: 5.976e1

GenotypeQuality
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bin: 2.5e0
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: 14

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.098887589577524e-4
allele num: 66702
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.949e1

VQSLOD
type: SiteQuality
SIO_000300: 2.55e0

QD
type: SiteQuality
SIO_000300: 1.242e1

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.141e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 1.104e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.54e-1

DP
type: SiteQuality
SIO_000300: 1.770406e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.24e-1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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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: 1

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

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

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

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.72e0

MQ
type: SiteQuality
SIO_000300: 3.678e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.367e0

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

QD
type: SiteQuality
SIO_000300: 1.642e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

DP
type: SiteQuality
SIO_000300: 1.769534e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 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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variant carriers: 0

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

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

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.769807e6

MQ
type: SiteQuality
SIO_000300: 5.944e1

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.44e-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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variant carriers: 6

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.993884158772035e-5
allele num: 66712
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e-1

DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -2.84e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.956e1

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: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

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

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

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

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

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.58e-1

ReadPosRankSum
type: SiteQuality
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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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variant carriers: 2

GenotypeQuality
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variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
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African
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allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498935755613514e-5
allele num: 66714
num of homozygotes: 0

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

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

Other
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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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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.953e1

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
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QD
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
type: SiteQuality
SIO_000300: -5.1e-1

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e-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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East Asian
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allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.24e-1

MQ
type: SiteQuality
SIO_000300: 5.595e1

FS
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ClippingRankSum
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BaseQRankSum
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QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.768749e6

VQSLOD
type: SiteQuality
SIO_000300: -3.8e-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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variant carriers: 2

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

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

African
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allele count: 2
allele frequency: 1.923446816695518e-4
allele num: 10398
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66702
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Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.767948e6

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.38e-1

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.68e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

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

MQRankSum
type: SiteQuality
SIO_000300: -4.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.818e0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66380
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East Asian
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allele frequency: 0.0e0
allele num: 8644
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African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 3
allele frequency: 2.593360995850622e-4
allele num: 11568
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.128e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.09e-1

DP
type: SiteQuality
SIO_000300: 1.80757e6

FS
type: SiteQuality
SIO_000300: 4.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.88e-1

QD
type: SiteQuality
SIO_000300: 1.225e1

VQSLOD
type: SiteQuality
SIO_000300: 2.19e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 5
allele frequency: 9.968102073365231e-4
allele num: 5016
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 2.298850574712644e-4
allele num: 8700
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.195028680688336e-4
allele num: 8368
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European (Non-Finnish)
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allele count: 33
allele frequency: 5.479179119346483e-4
allele num: 60228
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 2
allele frequency: 2.583979328165375e-3
allele num: 774
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.36e0

MQRankSum
type: SiteQuality
SIO_000300: -2.91e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.222e2

DP
type: SiteQuality
SIO_000300: 1.845188e6

QD
type: SiteQuality
SIO_000300: 2.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.48e-2

MQ
type: SiteQuality
SIO_000300: 5.876e1

FS
type: SiteQuality
SIO_000300: 3.00185e2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.114e0

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 2
allele frequency: 1.967729240456513e-4
allele num: 10164
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.116071428571429e-3
allele num: 896
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.040106305870983e-5
allele num: 66224
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16508
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European (Finnish)
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allele count: 2
allele frequency: 3.078817733990148e-4
allele num: 6496
num of homozygotes: 0

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

East Asian
type: Population
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allele frequency: 0.0e0
allele num: 8650
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MQ
type: SiteQuality
SIO_000300: 5.867e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ClippingRankSum
type: SiteQuality
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VQSLOD
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MQRankSum
type: SiteQuality
SIO_000300: -9.6e-2

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
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BaseQRankSum
type: SiteQuality
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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African
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South Asian
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allele frequency: 6.05766900896535e-5
allele num: 16508
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East Asian
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.500555205426008e-5
allele num: 66642
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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BaseQRankSum
type: SiteQuality
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DP
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MQRankSum
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FS
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MQ
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
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South Asian
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African
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allele frequency: 9.633911368015414e-5
allele num: 10380
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66630
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East Asian
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Other
type: Population
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MQ
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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QD
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ReadPosRankSum
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VQSLOD
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Finnish)
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East Asian
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South Asian
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European (Non-Finnish)
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allele num: 66630
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Other
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QD
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BaseQRankSum
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ClippingRankSum
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DP
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FS
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 6.05913717886573e-5
allele num: 16504
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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African
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Other
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East Asian
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

VQSLOD
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MQRankSum
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SIO_000300: 1.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.58e0

FS
type: SiteQuality
SIO_000300: 9.25e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.712084e6

QD
type: SiteQuality
SIO_000300: 1.432e1

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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bin: 9.75e1
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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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bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5004651441947e-5
allele num: 66646
num of homozygotes: 0

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.888e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

FS
type: SiteQuality
SIO_000300: 4.656e0

DP
type: SiteQuality
SIO_000300: 1.712447e6

VQSLOD
type: SiteQuality
SIO_000300: 7.13e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

InbreedingCoeff
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SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500645277469312e-5
allele num: 66638
num of homozygotes: 0

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

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 902
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

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

DP
type: SiteQuality
SIO_000300: 1.712459e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: -3.8e-2

InbreedingCoeff
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SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.7e-2

QD
type: SiteQuality
SIO_000300: 8.73e0

GenotypeQuality
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variant carriers: 0

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

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

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

South Asian
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allele count: 1
allele frequency: 6.062810719049351e-5
allele num: 16494
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66650
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.105e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e-1

FS
type: SiteQuality
SIO_000300: 5.997e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.07e-1

VQSLOD
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SIO_000300: -1.648e0

MQ
type: SiteQuality
SIO_000300: 5.867e1

MQRankSum
type: SiteQuality
SIO_000300: -9.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.64e-1

DP
type: SiteQuality
SIO_000300: 1.71273e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
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variant carriers: 0

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

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

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

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

South Asian
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allele frequency: 6.063545961678389e-5
allele num: 16492
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500330072615976e-5
allele num: 66652
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.153e1

MQ
type: SiteQuality
SIO_000300: 5.907e1

VQSLOD
type: SiteQuality
SIO_000300: 4.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.37e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.712628e6

BaseQRankSum
type: SiteQuality
SIO_000300: -9.59e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500060002400096e-5
allele num: 66664
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.2e-1

BaseQRankSum
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SIO_000300: -1.263e0

DP
type: SiteQuality
SIO_000300: 1.713054e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.964e1

FS
type: SiteQuality
SIO_000300: 8.686999999999999e0

QD
type: SiteQuality
SIO_000300: 1.678e1

MQRankSum
type: SiteQuality
SIO_000300: -2.43e-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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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500105007350515e-5
allele num: 66662
num of homozygotes: 0

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.83e-1

FS
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
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QD
type: SiteQuality
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InbreedingCoeff
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.29e-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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variant carriers: 0

East Asian
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allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.923446816695518e-4
allele num: 10398
num of homozygotes: 0

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

Other
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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: 2
allele frequency: 3.000210014701029e-5
allele num: 66662
num of homozygotes: 0

South Asian
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allele count: 5
allele frequency: 3.031772980839195e-4
allele num: 16492
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

DP
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
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FS
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ReadPosRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.7e-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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6608
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.000300030003e-5
allele num: 66660
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Other
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BaseQRankSum
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MQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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DP
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66662
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6608
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East Asian
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African
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Other
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South Asian
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allele frequency: 3.032876379958753e-4
allele num: 16486
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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QD
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BaseQRankSum
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FS
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MQRankSum
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MQ
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DP
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66660
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

African
type: Population
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allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.54e-1

FS
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 1.712551e6

MQRankSum
type: SiteQuality
SIO_000300: 1.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.0e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

QD
type: SiteQuality
SIO_000300: 1.157e1

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500240038406145e-5
allele num: 66656
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
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

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

DP
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 8.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.955e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500060002400096e-5
allele num: 66664
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
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African
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allele count: 0
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Latino
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allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.436e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.47e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.504e0

DP
type: SiteQuality
SIO_000300: 1.709235e6

VQSLOD
type: SiteQuality
SIO_000300: -2.04e0

MQRankSum
type: SiteQuality
SIO_000300: -9.72e-1

QD
type: SiteQuality
SIO_000300: 2.943e1

MQ
type: SiteQuality
SIO_000300: 5.934e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.9e-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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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.086427267194157e-5
allele num: 16430
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQRankSum
type: SiteQuality
SIO_000300: 4.74e-1

DP
type: SiteQuality
SIO_000300: 1.70584e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.962e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.116e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.2e-1

FS
type: SiteQuality
SIO_000300: 9.050000000000001e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.28e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 514
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 42
allele frequency: 6.303466906798739e-4
allele num: 66630
num of homozygotes: 1

Latino
type: Population
allele count: 12
allele frequency: 1.038062283737024e-3
allele num: 11560
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16400
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.941e1

QD
type: SiteQuality
SIO_000300: 1.513e1

DP
type: SiteQuality
SIO_000300: 1.703793e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.05e0

FS
type: SiteQuality
SIO_000300: 1.123e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.66e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.56e-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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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: 4

GenotypeQuality
all individuals: 1177
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66630
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 4
allele frequency: 2.439024390243902e-4
allele num: 16400
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.05e0

FS
type: SiteQuality
SIO_000300: 1.123e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.56e-1

QD
type: SiteQuality
SIO_000300: 1.513e1

MQRankSum
type: SiteQuality
SIO_000300: 1.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.66e-2

MQ
type: SiteQuality
SIO_000300: 5.941e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.85e-1

DP
type: SiteQuality
SIO_000300: 1.703793e6

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66646
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.92270717169775e-4
allele num: 10402
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16394
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.701443e6

BaseQRankSum
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ClippingRankSum
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SIO_000300: -5.649999999999999e-1

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.901e1

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16166
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.730403183941858e-4
allele num: 11558
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66554
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.648e0

VQSLOD
type: SiteQuality
SIO_000300: 6.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 5.89e-1

MQ
type: SiteQuality
SIO_000300: 5.949e1

BaseQRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
type: Population
allele count: 0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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African
type: Population
allele count: 1
allele frequency: 9.619084263178146e-5
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66532
num of homozygotes: 0

South Asian
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FS
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 413
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variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.730702665282105e-4
allele num: 11556
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15902
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66450
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.685643e6

VQSLOD
type: SiteQuality
SIO_000300: -3.974e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e-1

FS
type: SiteQuality
SIO_000300: 9.696999999999999e0

MQRankSum
type: SiteQuality
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MQ
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SIO_000300: 5.948e1

BaseQRankSum
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SIO_000300: -1.574e0

QD
type: SiteQuality
SIO_000300: 1.325e1

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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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

African
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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
allele num: 8650
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15612
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.507113576079093e-5
allele num: 66352
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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QD
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-2

VQSLOD
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MQRankSum
type: SiteQuality
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MQ
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.679433e6

FS
type: SiteQuality
SIO_000300: 7.51e-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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variant carriers: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.019597185735423e-5
allele num: 66234
num of homozygotes: 0

DP
type: SiteQuality
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ReadPosRankSum
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FS
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SIO_000300: 0.0e0

QD
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VQSLOD
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SIO_000300: 3.05e-1

ClippingRankSum
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InbreedingCoeff
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SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.89e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.257e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 88

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

East Asian
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allele count: 87
allele frequency: 1.007177587404492e-2
allele num: 8638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65642
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10246
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
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allele count: 1
allele frequency: 1.160092807424594e-3
allele num: 862
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.907e1

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.489e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: 5.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.78e0

DP
type: SiteQuality
SIO_000300: 1.641077e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65642
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13998
num of homozygotes: 0

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

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

African
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allele count: 1
allele frequency: 9.759906304899473e-5
allele num: 10246
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.248e1

MQRankSum
type: SiteQuality
SIO_000300: 2.22e-1

MQ
type: SiteQuality
SIO_000300: 5.907e1

VQSLOD
type: SiteQuality
SIO_000300: 2.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.489e0

DP
type: SiteQuality
SIO_000300: 1.641077e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13930
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524157902758726e-5
allele num: 65610
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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QD
type: SiteQuality
SIO_000300: 1.445e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.17e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.587e0

FS
type: SiteQuality
SIO_000300: 4.201e0

DP
type: SiteQuality
SIO_000300: 1.636526e6

MQRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.72e0

MQ
type: SiteQuality
SIO_000300: 5.805e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13592
num of homozygotes: 0

African
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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: 1
allele frequency: 1.528070657987225e-5
allele num: 65442
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6532
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East Asian
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allele frequency: 0.0e0
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Other
type: Population
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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QD
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ClippingRankSum
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SIO_000300: -1.002e0

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.538272212650751e-5
allele num: 65008
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Other
type: Population
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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QD
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DP
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.43e-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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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6454
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.541972491210757e-5
allele num: 64852
num of homozygotes: 0

Latino
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East Asian
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Other
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South Asian
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allele frequency: 0.0e0
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VQSLOD
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DP
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MQ
type: SiteQuality
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QD
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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MQRankSum
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FS
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

Latino
type: Population
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African
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 1.547364837681428e-5
allele num: 64626
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East Asian
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South Asian
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BaseQRankSum
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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FS
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DP
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InbreedingCoeff
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QD
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ClippingRankSum
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VQSLOD
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1296
bin: 9.75e1
variant carriers: 5

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11434
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.010305112143867e-4
allele num: 9898
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6408
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.201935003721161e-5
allele num: 64496
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.098e1

FS
type: SiteQuality
SIO_000300: 1.878e0

MQ
type: SiteQuality
SIO_000300: 5.883e1

DP
type: SiteQuality
SIO_000300: 1.591245e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.47e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 9.6e-1

GenotypeQuality
all individuals: 150
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1378
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11180
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64326
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6380
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11418
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9840
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.171508903467666e-4
allele num: 8536
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.66e-1

QD
type: SiteQuality
SIO_000300: 9.75e0

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

FS
type: SiteQuality
SIO_000300: 2.424e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.468e0

DP
type: SiteQuality
SIO_000300: 1.583716e6

MQ
type: SiteQuality
SIO_000300: 5.956e1

GenotypeQuality
all individuals: 367
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.25e1
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
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 73
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GenotypeQuality
all individuals: 1279
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9694
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6316
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8472
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 768
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.568233855032463e-5
allele num: 63766
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.072e1

DP
type: SiteQuality
SIO_000300: 1.559017e6

MQRankSum
type: SiteQuality
SIO_000300: 1.82e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.827e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.79e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.699e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.19e-1

GenotypeQuality
all individuals: 9221
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
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variant carriers: 0

GenotypeQuality
all individuals: 84
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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: 5.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1273
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 458
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variant carriers: 0

GenotypeQuality
all individuals: 2234
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.821453775582216e-5
allele num: 11336
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9686
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10158
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8462
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 768
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6306
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63718
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.02e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.812e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.789e0

QD
type: SiteQuality
SIO_000300: 5.07e0

MQ
type: SiteQuality
SIO_000300: 5.813e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.51e0

FS
type: SiteQuality
SIO_000300: 4.536e0

DP
type: SiteQuality
SIO_000300: 1.556655e6

GenotypeQuality
all individuals: 774
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2153
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 3.75e1
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GenotypeQuality
all individuals: 353
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2878
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GenotypeQuality
all individuals: 164
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GenotypeQuality
all individuals: 995
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9536
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 756
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11250
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.1649575895683e-5
allele num: 63192
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9568
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6260
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.729e-1

MQ
type: SiteQuality
SIO_000300: 5.889e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.41e-1

FS
type: SiteQuality
SIO_000300: 1.755e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

QD
type: SiteQuality
SIO_000300: 1.321e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.51e-1

DP
type: SiteQuality
SIO_000300: 1.522536e6

GenotypeQuality
all individuals: 789
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4788
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variant carriers: 0

GenotypeQuality
all individuals: 5369
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 591
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variant carriers: 0

GenotypeQuality
all individuals: 414
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GenotypeQuality
all individuals: 1240
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 307
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1372
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8145
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5960
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9086
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8128
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 726
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.634360801490537e-5
allele num: 61186
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10754
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.9e-2

MQ
type: SiteQuality
SIO_000300: 5.889e1

QD
type: SiteQuality
SIO_000300: 1.994e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.848e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.95e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.4e-1

DP
type: SiteQuality
SIO_000300: 1.19065e6

GenotypeQuality
all individuals: 836
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 764
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 800
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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
all individuals: 1559
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GenotypeQuality
all individuals: 7305
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8984
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10616
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8350
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.649511744523621e-5
allele num: 60624
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5876
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8052
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 716
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.727e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.691e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 5.481e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.04e-1

QD
type: SiteQuality
SIO_000300: 3.009e1

DP
type: SiteQuality
SIO_000300: 1.134155e6

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 764
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10584
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.388888888888889e-3
allele num: 720
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8978
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60534
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8296
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8038
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5874
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

VQSLOD
type: SiteQuality
SIO_000300: -2.799e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.358e0

DP
type: SiteQuality
SIO_000300: 1.126766e6

QD
type: SiteQuality
SIO_000300: 2.67e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.419999999999999e-1

GenotypeQuality
all individuals: 2382
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6283
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1101
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GenotypeQuality
all individuals: 5395
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8774
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10178
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7780
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.69468546637744e-5
allele num: 59008
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8046
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5704
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.194e0

DP
type: SiteQuality
SIO_000300: 1.07741e6

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 9.360000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

QD
type: SiteQuality
SIO_000300: 7.9e0

VQSLOD
type: SiteQuality
SIO_000300: -1.232e0

MQRankSum
type: SiteQuality
SIO_000300: 1.9e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.68e0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7436
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4256
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.878004807692308e-5
allele num: 53248
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.54e0

VQSLOD
type: SiteQuality
SIO_000300: 4.07e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

FS
type: SiteQuality
SIO_000300: 3.233e0

QD
type: SiteQuality
SIO_000300: 1.022e1

DP
type: SiteQuality
SIO_000300: 9.84889e5

MQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.35e-1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7214
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7410
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.08e1

FS
type: SiteQuality
SIO_000300: 5.622e0

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

DP
type: SiteQuality
SIO_000300: 9.89652e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53116
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4214
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9708
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 680
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.067e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-1

FS
type: SiteQuality
SIO_000300: 1.187e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.9322e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.38e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.52e0

MQRankSum
type: SiteQuality
SIO_000300: 2.82e-1

QD
type: SiteQuality
SIO_000300: 1.026e1

South Asian
type: Population
allele count: 4
allele frequency: 2.888503755054881e-4
allele num: 13848
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53116
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9708
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 680
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-1

FS
type: SiteQuality
SIO_000300: 1.187e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.067e0

MQRankSum
type: SiteQuality
SIO_000300: 2.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.38e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.52e0

QD
type: SiteQuality
SIO_000300: 1.026e1

DP
type: SiteQuality
SIO_000300: 9.9322e5

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13862
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7224
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7440
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.945e0

MQRankSum
type: SiteQuality
SIO_000300: 1.55e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

QD
type: SiteQuality
SIO_000300: 5.03e0

FS
type: SiteQuality
SIO_000300: 6.107e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.96e-1

DP
type: SiteQuality
SIO_000300: 9.9596e5

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7218
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13854
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4230
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

QD
type: SiteQuality
SIO_000300: 1.386e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.3e-2

FS
type: SiteQuality
SIO_000300: 4.747e0

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

DP
type: SiteQuality
SIO_000300: 1.002371e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53382
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9746
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.378929950358522e-4
allele num: 7252
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4274
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.708e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.42e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.34e-1

DP
type: SiteQuality
SIO_000300: 1.034816e6

MQRankSum
type: SiteQuality
SIO_000300: -1.025e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.828e0

QD
type: SiteQuality
SIO_000300: 6.39e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

South Asian
type: Population
allele count: 2
allele frequency: 1.412628902387343e-4
allele num: 14158
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.840909090909091e-3
allele num: 704
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9964
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7524
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7670
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 7.296607077708865e-5
allele num: 54820
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.0005e1

MQRankSum
type: SiteQuality
SIO_000300: 1.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

DP
type: SiteQuality
SIO_000300: 1.150398e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.18e0

VQSLOD
type: SiteQuality
SIO_000300: -4.521e-1

QD
type: SiteQuality
SIO_000300: 1.064e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.0e-2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7662
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9998
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14196
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 706
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.818446319464649e-5
allele num: 54992
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.22e-1

QD
type: SiteQuality
SIO_000300: 4.12e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.33e-1

DP
type: SiteQuality
SIO_000300: 1.158396e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.59e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.548e0