16-49672114-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672114
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672114
    reference: chr 16
allele count: 1
allele frequency: 8.251505899826718e-6
allele num: 121190
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.598G>C
  hgvsp: ENSP00000442321.1:p.Ala200Pro
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.598G>C
  hgvsp: ENSP00000455061.1:p.Ala200Pro
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.949G>C
  hgvsp: ENSP00000455426.1:p.Ala317Pro
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.949G>C
  hgvsp: ENSP00000262383.2:p.Ala317Pro
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.769G>C
  hgvsp: ENSP00000455588.2:p.Ala257Pro
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.769G>C
  hgvsp: ENSP00000457664.1:p.Ala257Pro
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.769G>C
  hgvsp: ENSP00000457928.1:p.Ala257Pro
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20148
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1081
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36139
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala317Pro
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

16-49672124-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672124
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672124
    reference: chr 16
allele count: 1
allele frequency: 8.252050634582693e-6
allele num: 121182
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.759T>C
  hgvsp: ENST00000562520.1:c.759T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.939T>C
  hgvsp: ENST00000262383.2:c.939T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.939T>C
  hgvsp: ENST00000561648.1:c.939T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.759T>C
  hgvsp: ENST00000563137.2:c.759T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.588T>C
  hgvsp: ENST00000535559.1:c.588T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.588T>C
  hgvsp: ENST00000567169.1:c.588T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.759T>C
  hgvsp: ENST00000562871.1:c.759T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10164
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20102
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36109
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 8.75e1
  variant carriers: 0
hgvs: p.His313His
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

16-49672129-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672129
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672129
    reference: chr 16
allele count: 2
allele frequency: 1.650437365901964e-5
allele num: 121180
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.583G>A
  hgvsp: ENSP00000442321.1:p.Ala195Thr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.583G>A
  hgvsp: ENSP00000455061.1:p.Ala195Thr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.754G>A
  hgvsp: ENSP00000455588.2:p.Ala252Thr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.934G>A
  hgvsp: ENSP00000455426.1:p.Ala312Thr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.934G>A
  hgvsp: ENSP00000262383.2:p.Ala312Thr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.754G>A
  hgvsp: ENSP00000457664.1:p.Ala252Thr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.754G>A
  hgvsp: ENSP00000457928.1:p.Ala252Thr
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10164
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20070
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1103
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3800
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala312Thr
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/16-49672131-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672131
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672131
    reference: chr 16
allele count: 1
allele frequency: 8.251233559417133e-6
allele num: 121194
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.752T>G
  hgvsp: ENSP00000455588.2:p.Leu251Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.932T>G
  hgvsp: ENSP00000262383.2:p.Leu311Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.752T>G
  hgvsp: ENSP00000457928.1:p.Leu251Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.932T>G
  hgvsp: ENSP00000455426.1:p.Leu311Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.581T>G
  hgvsp: ENSP00000455061.1:p.Leu194Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.581T>G
  hgvsp: ENSP00000442321.1:p.Leu194Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.752T>G
  hgvsp: ENSP00000457664.1:p.Leu251Arg
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3879
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10164
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20070
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2911
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9466
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1102
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36100
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu311Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum

16-49672145-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672145
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672145
    reference: chr 16
allele count: 17
allele frequency: 1.402732853653707e-4
allele num: 121192
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.918C>T
  hgvsp: ENST00000561648.1:c.918C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.567C>T
  hgvsp: ENST00000567169.1:c.567C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.738C>T
  hgvsp: ENST00000562871.1:c.738C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.738C>T
  hgvsp: ENST00000563137.2:c.738C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.567C>T
  hgvsp: ENST00000535559.1:c.567C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.918C>T
  hgvsp: ENST00000262383.2:c.918C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.738C>T
  hgvsp: ENST00000562520.1:c.738C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10169
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36016
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2926
  bin: 9.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 2209
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1082
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp306Asp
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD

16-49672147-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672147
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672147
    reference: chr 16
allele count: 2
allele frequency: 1.650328415354656e-5
allele num: 121188
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.916G>A
  hgvsp: ENSP00000262383.2:p.Asp306Asn
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.916G>A
  hgvsp: ENSP00000455426.1:p.Asp306Asn
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.736G>A
  hgvsp: ENSP00000457664.1:p.Asp246Asn
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.736G>A
  hgvsp: ENSP00000455588.2:p.Asp246Asn
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.565G>A
  hgvsp: ENSP00000442321.1:p.Asp189Asn
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.565G>A
  hgvsp: ENSP00000455061.1:p.Asp189Asn
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.736G>A
  hgvsp: ENSP00000457928.1:p.Asp246Asn
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22572
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9452
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35972
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3804
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp306Asn
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

16-49672148-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672148
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672148
    reference: chr 16
allele count: 2
allele frequency: 1.650137786505173e-5
allele num: 121202
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.915C>T
  hgvsp: ENST00000262383.2:c.915C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.735C>T
  hgvsp: ENST00000562520.1:c.735C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.735C>T
  hgvsp: ENST00000563137.2:c.735C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.564C>T
  hgvsp: ENST00000567169.1:c.564C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.915C>T
  hgvsp: ENST00000561648.1:c.915C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.564C>T
  hgvsp: ENST00000535559.1:c.564C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.735C>T
  hgvsp: ENST00000562871.1:c.735C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10174
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 36017
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2212
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val305Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

16-49672154-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672154
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672154
    reference: chr 16
allele count: 2
allele frequency: 1.650273945474949e-5
allele num: 121192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.729C>T
  hgvsp: ENST00000562871.1:c.729C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.729C>T
  hgvsp: ENST00000563137.2:c.729C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.909C>T
  hgvsp: ENST00000561648.1:c.909C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.558C>T
  hgvsp: ENST00000535559.1:c.558C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.729C>T
  hgvsp: ENST00000562520.1:c.729C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.558C>T
  hgvsp: ENST00000567169.1:c.558C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.909C>T
  hgvsp: ENST00000262383.2:c.909C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19940
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10181
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22565
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9463
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val303Val
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

16-49672157-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672157
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672157
    reference: chr 16
allele count: 1
allele frequency: 8.251642076773278e-6
allele num: 121188
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.726G>A
  hgvsp: ENST00000562871.1:c.726G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.726G>A
  hgvsp: ENST00000562520.1:c.726G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.555G>A
  hgvsp: ENST00000567169.1:c.555G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.906G>A
  hgvsp: ENST00000262383.2:c.906G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.906G>A
  hgvsp: ENST00000561648.1:c.906G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.726G>A
  hgvsp: ENST00000563137.2:c.726G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.555G>A
  hgvsp: ENST00000535559.1:c.555G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10172
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19930
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3801
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2210
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu302Glu
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

16-49672171-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672171
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672171
    reference: chr 16
allele count: 4
allele frequency: 3.30114714863415e-5
allele num: 121170
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.541A>T
  hgvsp: ENSP00000455061.1:p.Ile181Phe
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.892A>T
  hgvsp: ENSP00000262383.2:p.Ile298Phe
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.712A>T
  hgvsp: ENSP00000457664.1:p.Ile238Phe
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.712A>T
  hgvsp: ENSP00000455588.2:p.Ile238Phe
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.712A>T
  hgvsp: ENSP00000457928.1:p.Ile238Phe
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.892A>T
  hgvsp: ENSP00000455426.1:p.Ile298Phe
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.541A>T
  hgvsp: ENSP00000442321.1:p.Ile181Phe
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22581
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1085
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ile298Phe
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-49672171-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672171
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672171
    reference: chr 16
allele count: 2
allele frequency: 1.650573574317075e-5
allele num: 121170
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.712A>C
  hgvsp: ENSP00000457928.1:p.Ile238Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.892A>C
  hgvsp: ENSP00000262383.2:p.Ile298Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.892A>C
  hgvsp: ENSP00000455426.1:p.Ile298Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.541A>C
  hgvsp: ENSP00000442321.1:p.Ile181Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.541A>C
  hgvsp: ENSP00000455061.1:p.Ile181Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.712A>C
  hgvsp: ENSP00000455588.2:p.Ile238Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.712A>C
  hgvsp: ENSP00000457664.1:p.Ile238Leu
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22581
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9446
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35849
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1085
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2211
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile298Leu
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

16-49672175-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672175
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672175
    reference: chr 16
allele count: 1
allele frequency: 8.253549026081216e-6
allele num: 121160
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.708G>A
  hgvsp: ENST00000562520.1:c.708G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.708G>A
  hgvsp: ENST00000562871.1:c.708G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.537G>A
  hgvsp: ENST00000535559.1:c.537G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.888G>A
  hgvsp: ENST00000561648.1:c.888G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.708G>A
  hgvsp: ENST00000563137.2:c.708G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.537G>A
  hgvsp: ENST00000567169.1:c.537G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.888G>A
  hgvsp: ENST00000262383.2:c.888G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10176
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19773
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1089
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2928
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3791
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gln296Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

16-49672176-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672176
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672176
    reference: chr 16
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.707A>G
  hgvsp: ENSP00000455588.2:p.Gln236Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.536A>G
  hgvsp: ENSP00000455061.1:p.Gln179Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.707A>G
  hgvsp: ENSP00000457664.1:p.Gln236Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.887A>G
  hgvsp: ENSP00000455426.1:p.Gln296Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.536A>G
  hgvsp: ENSP00000442321.1:p.Gln179Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.887A>G
  hgvsp: ENSP00000262383.2:p.Gln296Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.707A>G
  hgvsp: ENSP00000457928.1:p.Gln236Arg
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19760
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10182
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2929
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3601
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gln296Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-49672181-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672181
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672181
    reference: chr 16
allele count: 1
allele frequency: 8.254094030639197e-6
allele num: 121152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.702C>A
  hgvsp: ENSP00000455588.2:p.Asp234Glu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.531C>A
  hgvsp: ENSP00000442321.1:p.Asp177Glu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.702C>A
  hgvsp: ENSP00000457664.1:p.Asp234Glu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.531C>A
  hgvsp: ENSP00000455061.1:p.Asp177Glu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.882C>A
  hgvsp: ENSP00000455426.1:p.Asp294Glu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.702C>A
  hgvsp: ENSP00000457928.1:p.Asp234Glu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.882C>A
  hgvsp: ENSP00000262383.2:p.Asp294Glu
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10197
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35604
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2929
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1103
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asp294Glu
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-49672182-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672182
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672182
    reference: chr 16
allele count: 2
allele frequency: 1.650873311982039e-5
allele num: 121148
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.881A>G
  hgvsp: ENSP00000262383.2:p.Asp294Gly
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.530A>G
  hgvsp: ENSP00000442321.1:p.Asp177Gly
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.701A>G
  hgvsp: ENSP00000457664.1:p.Asp234Gly
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.530A>G
  hgvsp: ENSP00000455061.1:p.Asp177Gly
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.881A>G
  hgvsp: ENSP00000455426.1:p.Asp294Gly
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.701A>G
  hgvsp: ENSP00000457928.1:p.Asp234Gly
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.701A>G
  hgvsp: ENSP00000455588.2:p.Asp234Gly
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10200
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19646
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3800
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1104
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3601
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35410
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp294Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

16-49672184-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672184
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672184
    reference: chr 16
allele count: 7
allele frequency: 5.778915215058202e-5
allele num: 121130
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.528G>A
  hgvsp: ENST00000535559.1:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.879G>A
  hgvsp: ENST00000561648.1:c.879G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.699G>A
  hgvsp: ENST00000562871.1:c.699G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.879G>A
  hgvsp: ENST00000262383.2:c.879G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.528G>A
  hgvsp: ENST00000567169.1:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.699G>A
  hgvsp: ENST00000562520.1:c.699G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.699G>A
  hgvsp: ENST00000563137.2:c.699G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3882
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2934
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 9414
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala293Ala
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff

16-49672185-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672185
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672185
    reference: chr 16
allele count: 3
allele frequency: 2.47639173215347e-5
allele num: 121144
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.527C>T
  hgvsp: ENSP00000455061.1:p.Ala176Val
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.527C>T
  hgvsp: ENSP00000442321.1:p.Ala176Val
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.878C>T
  hgvsp: ENSP00000455426.1:p.Ala293Val
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.698C>T
  hgvsp: ENSP00000457664.1:p.Ala233Val
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.698C>T
  hgvsp: ENSP00000457928.1:p.Ala233Val
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.878C>T
  hgvsp: ENSP00000262383.2:p.Ala293Val
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.698C>T
  hgvsp: ENSP00000455588.2:p.Ala233Val
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3879
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10231
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala293Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum

16-49672192-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672192
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672192
    reference: chr 16
allele count: 1
allele frequency: 8.257501940512956e-6
allele num: 121102
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.871G>A
  hgvsp: ENSP00000262383.2:p.Glu291Lys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.691G>A
  hgvsp: ENSP00000455588.2:p.Glu231Lys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.520G>A
  hgvsp: ENSP00000455061.1:p.Glu174Lys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.520G>A
  hgvsp: ENSP00000442321.1:p.Glu174Lys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.871G>A
  hgvsp: ENSP00000455426.1:p.Glu291Lys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.691G>A
  hgvsp: ENSP00000457664.1:p.Glu231Lys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.691G>A
  hgvsp: ENSP00000457928.1:p.Glu231Lys
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22555
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3889
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10251
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3788
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2931
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9378
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35135
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu291Lys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ

16-49672193-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672193
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672193
    reference: chr 16
allele count: 2
allele frequency: 1.651500388102591e-5
allele num: 121102
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.519C>T
  hgvsp: ENST00000535559.1:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.870C>T
  hgvsp: ENST00000262383.2:c.870C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.690C>T
  hgvsp: ENST00000562871.1:c.690C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.690C>T
  hgvsp: ENST00000563137.2:c.690C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.519C>T
  hgvsp: ENST00000567169.1:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.870C>T
  hgvsp: ENST00000561648.1:c.870C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.690C>T
  hgvsp: ENST00000562520.1:c.690C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10233
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9390
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3792
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser290Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

16-49672193-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672193
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672193
    reference: chr 16
allele count: 1
allele frequency: 8.257501940512956e-6
allele num: 121102
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.690C>A
  hgvsp: ENST00000562520.1:c.690C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.519C>A
  hgvsp: ENST00000567169.1:c.519C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.690C>A
  hgvsp: ENST00000562871.1:c.690C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.690C>A
  hgvsp: ENST00000563137.2:c.690C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.870C>A
  hgvsp: ENST00000561648.1:c.870C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.870C>A
  hgvsp: ENST00000262383.2:c.870C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.519C>A
  hgvsp: ENST00000535559.1:c.519C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10233
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1088
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35249
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3792
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser290Ser
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-49672202-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672202
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672202
    reference: chr 16
allele count: 2
allele frequency: 1.65188231990353e-5
allele num: 121074
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.510G>A
  hgvsp: ENST00000567169.1:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.861G>A
  hgvsp: ENST00000262383.2:c.861G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.861G>A
  hgvsp: ENST00000561648.1:c.861G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.681G>A
  hgvsp: ENST00000562520.1:c.681G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.510G>A
  hgvsp: ENST00000535559.1:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.681G>A
  hgvsp: ENST00000563137.2:c.681G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.681G>A
  hgvsp: ENST00000562871.1:c.681G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19149
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2213
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2934
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3788
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro287Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-49672203-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672203
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672203
    reference: chr 16
allele count: 1
allele frequency: 8.259684480052863e-6
allele num: 121070
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.860C>T
  hgvsp: ENSP00000262383.2:p.Pro287Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.680C>T
  hgvsp: ENSP00000457664.1:p.Pro227Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.509C>T
  hgvsp: ENSP00000442321.1:p.Pro170Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.860C>T
  hgvsp: ENSP00000455426.1:p.Pro287Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.509C>T
  hgvsp: ENSP00000455061.1:p.Pro170Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.680C>T
  hgvsp: ENSP00000455588.2:p.Pro227Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.680C>T
  hgvsp: ENSP00000457928.1:p.Pro227Leu
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34913
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9338
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro287Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

16-49672205-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672205
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672205
    reference: chr 16
allele count: 3
allele frequency: 2.477618843117175e-5
allele num: 121084
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.678C>T
  hgvsp: ENST00000563137.2:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.507C>T
  hgvsp: ENST00000535559.1:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.678C>T
  hgvsp: ENST00000562871.1:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.507C>T
  hgvsp: ENST00000567169.1:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.858C>T
  hgvsp: ENST00000262383.2:c.858C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.678C>T
  hgvsp: ENST00000562520.1:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.858C>T
  hgvsp: ENST00000561648.1:c.858C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10291
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22584
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35106
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2938
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
hgvs: p.His286His
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS

16-49672209-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672209
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672209
    reference: chr 16
allele count: 8
allele frequency: 6.609712973214139e-5
allele num: 121034
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.674G>A
  hgvsp: ENSP00000457928.1:p.Arg225His
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.674G>A
  hgvsp: ENSP00000455588.2:p.Arg225His
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.503G>A
  hgvsp: ENSP00000455061.1:p.Arg168His
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.854G>A
  hgvsp: ENSP00000455426.1:p.Arg285His
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.854G>A
  hgvsp: ENSP00000262383.2:p.Arg285His
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.503G>A
  hgvsp: ENSP00000442321.1:p.Arg168His
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.674G>A
  hgvsp: ENSP00000457664.1:p.Arg225His
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10305
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22523
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2945
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2216
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1091
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg285His
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-49672210-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672210
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672210
    reference: chr 16
allele count: 3
allele frequency: 2.47827379968939e-5
allele num: 121052
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.673C>T
  hgvsp: ENSP00000455588.2:p.Arg225Cys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.673C>T
  hgvsp: ENSP00000457664.1:p.Arg225Cys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.502C>T
  hgvsp: ENSP00000455061.1:p.Arg168Cys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.853C>T
  hgvsp: ENSP00000262383.2:p.Arg285Cys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.853C>T
  hgvsp: ENSP00000455426.1:p.Arg285Cys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.673C>T
  hgvsp: ENSP00000457928.1:p.Arg225Cys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.502C>T
  hgvsp: ENSP00000442321.1:p.Arg168Cys
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10278
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34894
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg285Cys
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

16-49672214-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672214
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672214
    reference: chr 16
allele count: 1
allele frequency: 8.260776182530111e-6
allele num: 121054
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.669C>T
  hgvsp: ENST00000562871.1:c.669C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.849C>T
  hgvsp: ENST00000561648.1:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.849C>T
  hgvsp: ENST00000262383.2:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.669C>T
  hgvsp: ENST00000563137.2:c.669C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.498C>T
  hgvsp: ENST00000535559.1:c.498C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.669C>T
  hgvsp: ENST00000562520.1:c.669C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.498C>T
  hgvsp: ENST00000567169.1:c.498C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3932
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22538
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9391
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3626
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu283Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

16-49672216-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672216
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672216
    reference: chr 16
allele count: 1
allele frequency: 8.261185645363822e-6
allele num: 121048
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.667C>A
  hgvsp: ENSP00000457664.1:p.Leu223Ile
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.667C>A
  hgvsp: ENSP00000455588.2:p.Leu223Ile
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.847C>A
  hgvsp: ENSP00000262383.2:p.Leu283Ile
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.496C>A
  hgvsp: ENSP00000442321.1:p.Leu166Ile
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.496C>A
  hgvsp: ENSP00000455061.1:p.Leu166Ile
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.667C>A
  hgvsp: ENSP00000457928.1:p.Leu223Ile
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.847C>A
  hgvsp: ENSP00000455426.1:p.Leu283Ile
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1887
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2235
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3627
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu283Ile
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

16-49672219-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672219
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672219
    reference: chr 16
allele count: 2
allele frequency: 1.652701340340787e-5
allele num: 121014
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.493G>A
  hgvsp: ENSP00000455061.1:p.Val165Met
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.664G>A
  hgvsp: ENSP00000457664.1:p.Val222Met
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.664G>A
  hgvsp: ENSP00000457928.1:p.Val222Met
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.844G>A
  hgvsp: ENSP00000262383.2:p.Val282Met
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.844G>A
  hgvsp: ENSP00000455426.1:p.Val282Met
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.664G>A
  hgvsp: ENSP00000455588.2:p.Val222Met
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.493G>A
  hgvsp: ENSP00000442321.1:p.Val165Met
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10303
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3939
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22540
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3811
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3628
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1108
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34834
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val282Met
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

16-49672220-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672220
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672220
    reference: chr 16
allele count: 1
allele frequency: 8.262414277451872e-6
allele num: 121030
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.492C>T
  hgvsp: ENST00000567169.1:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.843C>T
  hgvsp: ENST00000561648.1:c.843C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.843C>T
  hgvsp: ENST00000262383.2:c.843C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.492C>T
  hgvsp: ENST00000535559.1:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.663C>T
  hgvsp: ENST00000563137.2:c.663C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.663C>T
  hgvsp: ENST00000562871.1:c.663C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.663C>T
  hgvsp: ENST00000562520.1:c.663C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10295
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22573
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3808
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9399
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34964
  bin: 6.25e1
  variant carriers: 0
hgvs: p.His281His
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-49672223-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672223
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672223
    reference: chr 16
allele count: 2
allele frequency: 1.652537471287161e-5
allele num: 121026
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.840G>A
  hgvsp: ENST00000561648.1:c.840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.660G>A
  hgvsp: ENST00000563137.2:c.660G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.660G>A
  hgvsp: ENST00000562520.1:c.660G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.489G>A
  hgvsp: ENST00000567169.1:c.489G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.840G>A
  hgvsp: ENST00000262383.2:c.840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.489G>A
  hgvsp: ENST00000535559.1:c.489G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.660G>A
  hgvsp: ENST00000562871.1:c.660G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3955
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2954
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9400
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3621
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Lys280Lys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

16-49672238-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672238
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672238
    reference: chr 16
allele count: 1
allele frequency: 8.268152729317216e-6
allele num: 120946
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.645G>A
  hgvsp: ENST00000563137.2:c.645G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.645G>A
  hgvsp: ENST00000562520.1:c.645G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.474G>A
  hgvsp: ENST00000567169.1:c.474G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.825G>A
  hgvsp: ENST00000561648.1:c.825G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.645G>A
  hgvsp: ENST00000562871.1:c.645G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.825G>A
  hgvsp: ENST00000262383.2:c.825G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.474G>A
  hgvsp: ENST00000535559.1:c.474G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3984
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18907
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr275Thr
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-49672239-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672239
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672239
    reference: chr 16
allele count: 5
allele frequency: 4.134213093879711e-5
allele num: 120942
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.644C>T
  hgvsp: ENSP00000457664.1:p.Thr215Met
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.644C>T
  hgvsp: ENSP00000457928.1:p.Thr215Met
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.644C>T
  hgvsp: ENSP00000455588.2:p.Thr215Met
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.824C>T
  hgvsp: ENSP00000262383.2:p.Thr275Met
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.473C>T
  hgvsp: ENSP00000455061.1:p.Thr158Met
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.473C>T
  hgvsp: ENSP00000442321.1:p.Thr158Met
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.824C>T
  hgvsp: ENSP00000455426.1:p.Thr275Met
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10396
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3984
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18895
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3654
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1121
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2259
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3837
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr275Met
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-49672245-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672245
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672245
    reference: chr 16
allele count: 1
allele frequency: 8.271298593879239e-6
allele num: 120900
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.818G>C
  hgvsp: ENSP00000455426.1:p.Ser273Thr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.467G>C
  hgvsp: ENSP00000455061.1:p.Ser156Thr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.818G>C
  hgvsp: ENSP00000262383.2:p.Ser273Thr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.638G>C
  hgvsp: ENSP00000455588.2:p.Ser213Thr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.467G>C
  hgvsp: ENSP00000442321.1:p.Ser156Thr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.638G>C
  hgvsp: ENSP00000457928.1:p.Ser213Thr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.638G>C
  hgvsp: ENSP00000457664.1:p.Ser213Thr
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3995
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10408
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34897
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2264
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1122
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2962
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser273Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

16-49672250-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672250
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672250
    reference: chr 16
allele count: 1
allele frequency: 8.274994621253496e-6
allele num: 120846
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.633C>T
  hgvsp: ENST00000562871.1:c.633C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.813C>T
  hgvsp: ENST00000561648.1:c.813C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.462C>T
  hgvsp: ENST00000567169.1:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.813C>T
  hgvsp: ENST00000262383.2:c.813C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.633C>T
  hgvsp: ENST00000563137.2:c.633C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.462C>T
  hgvsp: ENST00000535559.1:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.633C>T
  hgvsp: ENST00000562520.1:c.633C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3996
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34859
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9453
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3663
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr271Thr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

16-49672253-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672253
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672253
    reference: chr 16
allele count: 2
allele frequency: 1.655300271469245e-5
allele num: 120824
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.810C>T
  hgvsp: ENST00000262383.2:c.810C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.630C>T
  hgvsp: ENST00000562520.1:c.630C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.459C>T
  hgvsp: ENST00000567169.1:c.459C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.810C>T
  hgvsp: ENST00000561648.1:c.810C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.630C>T
  hgvsp: ENST00000562871.1:c.630C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.630C>T
  hgvsp: ENST00000563137.2:c.630C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.459C>T
  hgvsp: ENST00000535559.1:c.459C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3997
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22623
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3852
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asp270Asp
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD

16-49672255-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672255
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672255
    reference: chr 16
allele count: 1
allele frequency: 8.276912380605539e-6
allele num: 120818
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.457G>A
  hgvsp: ENSP00000455061.1:p.Asp153Asn
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.628G>A
  hgvsp: ENSP00000455588.2:p.Asp210Asn
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.628G>A
  hgvsp: ENSP00000457664.1:p.Asp210Asn
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.808G>A
  hgvsp: ENSP00000262383.2:p.Asp270Asn
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.808G>A
  hgvsp: ENSP00000455426.1:p.Asp270Asn
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.628G>A
  hgvsp: ENSP00000457928.1:p.Asp210Asn
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.457G>A
  hgvsp: ENSP00000442321.1:p.Asp153Asn
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22628
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18726
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10438
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3661
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1109
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp270Asn
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

16-49672258-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672258
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672258
    reference: chr 16
allele count: 1
allele frequency: 8.281024859636628e-6
allele num: 120758
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.625G>A
  hgvsp: ENSP00000457928.1:p.Glu209Lys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.805G>A
  hgvsp: ENSP00000455426.1:p.Glu269Lys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.454G>A
  hgvsp: ENSP00000442321.1:p.Glu152Lys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.805G>A
  hgvsp: ENSP00000262383.2:p.Glu269Lys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.625G>A
  hgvsp: ENSP00000455588.2:p.Glu209Lys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.454G>A
  hgvsp: ENSP00000455061.1:p.Glu152Lys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.625G>A
  hgvsp: ENSP00000457664.1:p.Glu209Lys
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18631
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22628
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3998
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9411
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3660
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1124
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2259
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu269Lys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

16-49672259-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672259
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672259
    reference: chr 16
allele count: 9
allele frequency: 7.453169253192441e-5
allele num: 120754
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.804C>T
  hgvsp: ENST00000561648.1:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.624C>T
  hgvsp: ENST00000562520.1:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.453C>T
  hgvsp: ENST00000567169.1:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.624C>T
  hgvsp: ENST00000562871.1:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.453C>T
  hgvsp: ENST00000535559.1:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.624C>T
  hgvsp: ENST00000563137.2:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.804C>T
  hgvsp: ENST00000262383.2:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10438
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22622
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2261
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3851
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 593
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1110
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Cys268Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

16-49672268-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672268
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672268
    reference: chr 16
allele count: 86
allele frequency: 7.124513296330047e-4
allele num: 120710
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.615C>T
  hgvsp: ENST00000562871.1:c.615C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.795C>T
  hgvsp: ENST00000561648.1:c.795C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.444C>T
  hgvsp: ENST00000567169.1:c.444C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.615C>T
  hgvsp: ENST00000562520.1:c.615C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.615C>T
  hgvsp: ENST00000563137.2:c.615C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.795C>T
  hgvsp: ENST00000262383.2:c.795C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.444C>T
  hgvsp: ENST00000535559.1:c.444C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4012
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 22608
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 10431
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18626
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1107
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1123
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9393
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Cys265Cys
num of homozygotes: 1
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

16-49672279-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672279
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672279
    reference: chr 16
allele count: 1
allele frequency: 8.29393713195654e-6
allele num: 120570
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.604G>A
  hgvsp: ENSP00000455588.2:p.Asp202Asn
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.784G>A
  hgvsp: ENSP00000455426.1:p.Asp262Asn
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.433G>A
  hgvsp: ENSP00000455061.1:p.Asp145Asn
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.433G>A
  hgvsp: ENSP00000442321.1:p.Asp145Asn
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.784G>A
  hgvsp: ENSP00000262383.2:p.Asp262Asn
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.604G>A
  hgvsp: ENSP00000457928.1:p.Asp202Asn
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.604G>A
  hgvsp: ENSP00000457664.1:p.Asp202Asn
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18498
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4012
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22556
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34617
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9397
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1110
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp262Asn
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

16-49672280-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672280
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672280
    reference: chr 16
allele count: 30
allele frequency: 2.488222413907504e-4
allele num: 120568
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.603C>T
  hgvsp: ENST00000562520.1:c.603C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.783C>T
  hgvsp: ENST00000262383.2:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.603C>T
  hgvsp: ENST00000562871.1:c.603C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.783C>T
  hgvsp: ENST00000561648.1:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.432C>T
  hgvsp: ENST00000535559.1:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.432C>T
  hgvsp: ENST00000567169.1:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.603C>T
  hgvsp: ENST00000563137.2:c.603C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18462
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4013
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10444
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22569
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 34602
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1130
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3662
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asp261Asp
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum

http://identifiers.org/exac.variant/16-49672282-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672282
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672282
    reference: chr 16
allele count: 6
allele frequency: 4.977105315548477e-5
allele num: 120552
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.430G>T
  hgvsp: ENSP00000442321.1:p.Asp144Tyr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.601G>T
  hgvsp: ENSP00000457664.1:p.Asp201Tyr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.601G>T
  hgvsp: ENSP00000455588.2:p.Asp201Tyr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.781G>T
  hgvsp: ENSP00000455426.1:p.Asp261Tyr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.601G>T
  hgvsp: ENSP00000457928.1:p.Asp201Tyr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.781G>T
  hgvsp: ENSP00000262383.2:p.Asp261Tyr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.430G>T
  hgvsp: ENSP00000455061.1:p.Asp144Tyr
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10441
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18469
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4013
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22555
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3873
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2994
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9405
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asp261Tyr
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP

16-49672287-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672287
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672287
    reference: chr 16
allele count: 1
allele frequency: 8.300270588821196e-6
allele num: 120478
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.776A>G
  hgvsp: ENSP00000262383.2:p.Lys259Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.596A>G
  hgvsp: ENSP00000457928.1:p.Lys199Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.596A>G
  hgvsp: ENSP00000455588.2:p.Lys199Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.776A>G
  hgvsp: ENSP00000455426.1:p.Lys259Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.596A>G
  hgvsp: ENSP00000457664.1:p.Lys199Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.425A>G
  hgvsp: ENSP00000455061.1:p.Lys142Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.425A>G
  hgvsp: ENSP00000442321.1:p.Lys142Arg
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10434
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22446
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4014
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34445
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 904
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3867
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Lys259Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

16-49672298-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672298
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672298
    reference: chr 16
allele count: 1
allele frequency: 8.313242996092776e-6
allele num: 120290
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.585G>A
  hgvsp: ENST00000563137.2:c.585G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.414G>A
  hgvsp: ENST00000535559.1:c.414G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.414G>A
  hgvsp: ENST00000567169.1:c.414G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.585G>A
  hgvsp: ENST00000562871.1:c.585G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.585G>A
  hgvsp: ENST00000562520.1:c.585G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.765G>A
  hgvsp: ENST00000561648.1:c.765G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.765G>A
  hgvsp: ENST00000262383.2:c.765G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10422
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22307
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18313
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1035
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1131
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34158
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu255Glu
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

16-49672302-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672302
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672302
    reference: chr 16
allele count: 4
allele frequency: 3.327067356478632e-5
allele num: 120226
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.410C>T
  hgvsp: ENSP00000455061.1:p.Ser137Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.410C>T
  hgvsp: ENSP00000442321.1:p.Ser137Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.581C>T
  hgvsp: ENSP00000455588.2:p.Ser194Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.581C>T
  hgvsp: ENSP00000457928.1:p.Ser194Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.761C>T
  hgvsp: ENSP00000262383.2:p.Ser254Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.581C>T
  hgvsp: ENSP00000457664.1:p.Ser194Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.761C>T
  hgvsp: ENSP00000455426.1:p.Ser254Leu
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22263
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10418
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18300
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4014
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3864
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3669
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1133
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser254Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: African
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

16-49672309-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672309
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672309
    reference: chr 16
allele count: 1
allele frequency: 8.321405984755183e-6
allele num: 120172
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.574G>A
  hgvsp: ENSP00000455588.2:p.Ala192Thr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.754G>A
  hgvsp: ENSP00000455426.1:p.Ala252Thr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.754G>A
  hgvsp: ENSP00000262383.2:p.Ala252Thr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.403G>A
  hgvsp: ENSP00000442321.1:p.Ala135Thr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.574G>A
  hgvsp: ENSP00000457664.1:p.Ala192Thr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.403G>A
  hgvsp: ENSP00000455061.1:p.Ala135Thr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.574G>A
  hgvsp: ENSP00000457928.1:p.Ala192Thr
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10415
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1073
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala252Thr
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ

16-49672312-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672312
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672312
    reference: chr 16
allele count: 1
allele frequency: 8.321544478655239e-6
allele num: 120170
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.571C>G
  hgvsp: ENSP00000457664.1:p.Leu191Val
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.400C>G
  hgvsp: ENSP00000442321.1:p.Leu134Val
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.571C>G
  hgvsp: ENSP00000457928.1:p.Leu191Val
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.400C>G
  hgvsp: ENSP00000455061.1:p.Leu134Val
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.751C>G
  hgvsp: ENSP00000455426.1:p.Leu251Val
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.571C>G
  hgvsp: ENSP00000455588.2:p.Leu191Val
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.751C>G
  hgvsp: ENSP00000262383.2:p.Leu251Val
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18236
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9391
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2276
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3671
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1137
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1108
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu251Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS

16-49672318-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672318
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672318
    reference: chr 16
allele count: 1
allele frequency: 8.32514693884347e-6
allele num: 120118
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.394G>A
  hgvsp: ENSP00000442321.1:p.Glu132Lys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.394G>A
  hgvsp: ENSP00000455061.1:p.Glu132Lys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.565G>A
  hgvsp: ENSP00000457928.1:p.Glu189Lys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.565G>A
  hgvsp: ENSP00000457664.1:p.Glu189Lys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.745G>A
  hgvsp: ENSP00000262383.2:p.Glu249Lys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.745G>A
  hgvsp: ENSP00000455426.1:p.Glu249Lys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.565G>A
  hgvsp: ENSP00000455588.2:p.Glu189Lys
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18234
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10418
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4016
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9392
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1141
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3867
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu249Lys
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS

16-49672322-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672322
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672322
    reference: chr 16
allele count: 1
allele frequency: 8.331111703545721e-6
allele num: 120032
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.390C>T
  hgvsp: ENST00000535559.1:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.741C>T
  hgvsp: ENST00000561648.1:c.741C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.741C>T
  hgvsp: ENST00000262383.2:c.741C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.561C>T
  hgvsp: ENST00000563137.2:c.561C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.561C>T
  hgvsp: ENST00000562871.1:c.561C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.390C>T
  hgvsp: ENST00000567169.1:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.561C>T
  hgvsp: ENST00000562520.1:c.561C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4017
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2280
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33971
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9383
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3668
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1137
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn247Asn
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

16-49672329-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672329
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672329
    reference: chr 16
allele count: 2
allele frequency: 1.666583337499792e-5
allele num: 120006
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.554A>G
  hgvsp: ENSP00000457928.1:p.Lys185Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.734A>G
  hgvsp: ENSP00000455426.1:p.Lys245Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.383A>G
  hgvsp: ENSP00000442321.1:p.Lys128Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.554A>G
  hgvsp: ENSP00000455588.2:p.Lys185Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.734A>G
  hgvsp: ENSP00000262383.2:p.Lys245Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.554A>G
  hgvsp: ENSP00000457664.1:p.Lys185Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.383A>G
  hgvsp: ENSP00000455061.1:p.Lys128Arg
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18209
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1110
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2994
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3670
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Lys245Arg
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

16-49672342-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672342
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672342
    reference: chr 16
allele count: 1
allele frequency: 8.337919188887221e-6
allele num: 119934
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.721A>C
  hgvsp: ENSP00000262383.2:p.Met241Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.541A>C
  hgvsp: ENSP00000455588.2:p.Met181Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.721A>C
  hgvsp: ENSP00000455426.1:p.Met241Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.541A>C
  hgvsp: ENSP00000457664.1:p.Met181Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.370A>C
  hgvsp: ENSP00000442321.1:p.Met124Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.541A>C
  hgvsp: ENSP00000457928.1:p.Met181Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.370A>C
  hgvsp: ENSP00000455061.1:p.Met124Leu
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18135
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1160
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33933
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2275
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Met241Leu
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ

16-49672344-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672344
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672344
    reference: chr 16
allele count: 1
allele frequency: 8.339170752860335e-6
allele num: 119916
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.719A>C
  hgvsp: ENSP00000262383.2:p.His240Pro
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.539A>C
  hgvsp: ENSP00000457928.1:p.His180Pro
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.539A>C
  hgvsp: ENSP00000455588.2:p.His180Pro
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.368A>C
  hgvsp: ENSP00000442321.1:p.His123Pro
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.539A>C
  hgvsp: ENSP00000457664.1:p.His180Pro
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.368A>C
  hgvsp: ENSP00000455061.1:p.His123Pro
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.719A>C
  hgvsp: ENSP00000455426.1:p.His240Pro
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10430
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1138
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2276
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9378
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2996
  bin: 9.75e1
  variant carriers: 1
hgvs: p.His240Pro
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

16-49672346-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672346
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672346
    reference: chr 16
allele count: 3
allele frequency: 2.502878310056565e-5
allele num: 119862
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.717C>T
  hgvsp: ENST00000561648.1:c.717C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.537C>T
  hgvsp: ENST00000563137.2:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.717C>T
  hgvsp: ENST00000262383.2:c.717C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.537C>T
  hgvsp: ENST00000562871.1:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.366C>T
  hgvsp: ENST00000567169.1:c.366C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.366C>T
  hgvsp: ENST00000535559.1:c.366C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.537C>T
  hgvsp: ENST00000562520.1:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18081
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4020
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22138
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10435
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9383
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33796
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3680
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1135
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1111
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser239Ser
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

16-49672349-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672349
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672349
    reference: chr 16
allele count: 1
allele frequency: 8.349475652928997e-6
allele num: 119768
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.363G>A
  hgvsp: ENST00000567169.1:c.363G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.714G>A
  hgvsp: ENST00000561648.1:c.714G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.534G>A
  hgvsp: ENST00000562871.1:c.534G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.534G>A
  hgvsp: ENST00000563137.2:c.534G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.534G>A
  hgvsp: ENST00000562520.1:c.534G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.714G>A
  hgvsp: ENST00000262383.2:c.714G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.363G>A
  hgvsp: ENST00000535559.1:c.363G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10418
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22121
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4020
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2275
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1102
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln238Gln
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-49672356-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672356
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672356
    reference: chr 16
allele count: 3
allele frequency: 2.504675394068929e-5
allele num: 119776
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.527C>T
  hgvsp: ENSP00000457928.1:p.Ser176Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.527C>T
  hgvsp: ENSP00000457664.1:p.Ser176Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.707C>T
  hgvsp: ENSP00000455426.1:p.Ser236Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.356C>T
  hgvsp: ENSP00000442321.1:p.Ser119Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.527C>T
  hgvsp: ENSP00000455588.2:p.Ser176Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.707C>T
  hgvsp: ENSP00000262383.2:p.Ser236Leu
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.356C>T
  hgvsp: ENSP00000455061.1:p.Ser119Leu
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1176
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9373
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1136
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33706
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser236Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-49672375-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672375
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672375
    reference: chr 16
allele count: 4
allele frequency: 3.341352579524191e-5
allele num: 119712
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.688G>A
  hgvsp: ENSP00000455426.1:p.Gly230Ser
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.508G>A
  hgvsp: ENSP00000455588.2:p.Gly170Ser
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.508G>A
  hgvsp: ENSP00000457664.1:p.Gly170Ser
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.337G>A
  hgvsp: ENSP00000442321.1:p.Gly113Ser
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.337G>A
  hgvsp: ENSP00000455061.1:p.Gly113Ser
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.688G>A
  hgvsp: ENSP00000262383.2:p.Gly230Ser
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.508G>A
  hgvsp: ENSP00000457928.1:p.Gly170Ser
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18018
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22133
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33702
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9374
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2276
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly230Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

16-49672376-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672376
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672376
    reference: chr 16
allele count: 291
allele frequency: 2.430509154082587e-3
allele num: 119728
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.336C>T
  hgvsp: ENST00000535559.1:c.336C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.687C>T
  hgvsp: ENST00000561648.1:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.687C>T
  hgvsp: ENST00000262383.2:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.507C>T
  hgvsp: ENST00000562871.1:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.507C>T
  hgvsp: ENST00000562520.1:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.507C>T
  hgvsp: ENST00000563137.2:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.336C>T
  hgvsp: ENST00000567169.1:c.336C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 4010
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 22045
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 4.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 10394
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 17970
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1109
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2261
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3859
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.25e1
  variant carriers: 1
hgvs: p.Arg229Arg
num of homozygotes: 4
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS

16-49672383-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672383
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672383
    reference: chr 16
allele count: 1
allele frequency: 8.354358468813179e-6
allele num: 119698
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.329G>A
  hgvsp: ENSP00000455061.1:p.Cys110Tyr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.500G>A
  hgvsp: ENSP00000457664.1:p.Cys167Tyr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.500G>A
  hgvsp: ENSP00000455588.2:p.Cys167Tyr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.500G>A
  hgvsp: ENSP00000457928.1:p.Cys167Tyr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.329G>A
  hgvsp: ENSP00000442321.1:p.Cys110Tyr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.680G>A
  hgvsp: ENSP00000455426.1:p.Cys227Tyr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.680G>A
  hgvsp: ENSP00000262383.2:p.Cys227Tyr
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18016
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22072
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4033
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1138
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33711
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1117
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Cys227Tyr
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

16-49672384-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672384
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672384
    reference: chr 16
allele count: 1
allele frequency: 8.353102342209896e-6
allele num: 119716
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.328T>C
  hgvsp: ENSP00000442321.1:p.Cys110Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.499T>C
  hgvsp: ENSP00000457928.1:p.Cys167Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.679T>C
  hgvsp: ENSP00000262383.2:p.Cys227Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.679T>C
  hgvsp: ENSP00000455426.1:p.Cys227Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.499T>C
  hgvsp: ENSP00000455588.2:p.Cys167Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.328T>C
  hgvsp: ENSP00000455061.1:p.Cys110Arg
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.499T>C
  hgvsp: ENSP00000457664.1:p.Cys167Arg
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4032
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22080
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3879
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1175
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Cys227Arg
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

16-49672392-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672392
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672392
    reference: chr 16
allele count: 1
allele frequency: 8.354777261638205e-6
allele num: 119692
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.491G>A
  hgvsp: ENSP00000455588.2:p.Cys164Tyr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.491G>A
  hgvsp: ENSP00000457664.1:p.Cys164Tyr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.320G>A
  hgvsp: ENSP00000442321.1:p.Cys107Tyr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.671G>A
  hgvsp: ENSP00000262383.2:p.Cys224Tyr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.671G>A
  hgvsp: ENSP00000455426.1:p.Cys224Tyr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.320G>A
  hgvsp: ENSP00000455061.1:p.Cys107Tyr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.491G>A
  hgvsp: ENSP00000457928.1:p.Cys164Tyr
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18024
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4038
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22085
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1116
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3094
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33795
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Cys224Tyr
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

16-49672394-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672394
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672394
    reference: chr 16
allele count: 1
allele frequency: 8.357430591538938e-6
allele num: 119654
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.489G>A
  hgvsp: ENST00000563137.2:c.489G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.489G>A
  hgvsp: ENST00000562520.1:c.489G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.318G>A
  hgvsp: ENST00000535559.1:c.318G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.669G>A
  hgvsp: ENST00000561648.1:c.669G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.489G>A
  hgvsp: ENST00000562871.1:c.489G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.318G>A
  hgvsp: ENST00000567169.1:c.318G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.669G>A
  hgvsp: ENST00000262383.2:c.669G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4039
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1116
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3882
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys223Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum

16-49672408-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672408
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672408
    reference: chr 16
allele count: 1
allele frequency: 8.355056480181806e-6
allele num: 119688
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.475A>G
  hgvsp: ENSP00000457928.1:p.Ser159Gly
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.475A>G
  hgvsp: ENSP00000455588.2:p.Ser159Gly
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.304A>G
  hgvsp: ENSP00000442321.1:p.Ser102Gly
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.655A>G
  hgvsp: ENSP00000455426.1:p.Ser219Gly
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.655A>G
  hgvsp: ENSP00000262383.2:p.Ser219Gly
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.304A>G
  hgvsp: ENSP00000455061.1:p.Ser102Gly
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.475A>G
  hgvsp: ENSP00000457664.1:p.Ser159Gly
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22072
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17992
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4040
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1120
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3681
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1146
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser219Gly
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-49672409-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672409
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672409
    reference: chr 16
allele count: 1
allele frequency: 8.356452852893003e-6
allele num: 119668
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.303C>T
  hgvsp: ENST00000535559.1:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.474C>T
  hgvsp: ENST00000563137.2:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.474C>T
  hgvsp: ENST00000562871.1:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.474C>T
  hgvsp: ENST00000562520.1:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.654C>T
  hgvsp: ENST00000561648.1:c.654C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.654C>T
  hgvsp: ENST00000262383.2:c.654C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.303C>T
  hgvsp: ENST00000567169.1:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4043
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1120
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33627
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1150
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9346
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser218Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

16-49672411-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672411
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672411
    reference: chr 16
allele count: 1
allele frequency: 8.356452852893003e-6
allele num: 119668
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.301T>A
  hgvsp: ENSP00000442321.1:p.Ser101Thr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.652T>A
  hgvsp: ENSP00000262383.2:p.Ser218Thr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.472T>A
  hgvsp: ENSP00000457928.1:p.Ser158Thr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.652T>A
  hgvsp: ENSP00000455426.1:p.Ser218Thr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.472T>A
  hgvsp: ENSP00000457664.1:p.Ser158Thr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.472T>A
  hgvsp: ENSP00000455588.2:p.Ser158Thr
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.301T>A
  hgvsp: ENSP00000455061.1:p.Ser101Thr
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4042
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10434
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22085
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17993
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1119
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3685
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2278
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1150
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser218Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

16-49672418-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672418
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672418
    reference: chr 16
allele count: 1
allele frequency: 8.354079296920687e-6
allele num: 119702
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.465C>T
  hgvsp: ENST00000562871.1:c.465C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.645C>T
  hgvsp: ENST00000561648.1:c.645C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.645C>T
  hgvsp: ENST00000262383.2:c.645C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.465C>T
  hgvsp: ENST00000563137.2:c.465C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.294C>T
  hgvsp: ENST00000567169.1:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.294C>T
  hgvsp: ENST00000535559.1:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.465C>T
  hgvsp: ENST00000562520.1:c.465C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22111
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17977
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3690
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3093
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr215Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum

16-49672427-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672427
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672427
    reference: chr 16
allele count: 1
allele frequency: 8.350451759440186e-6
allele num: 119754
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.456C>T
  hgvsp: ENST00000562871.1:c.456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.456C>T
  hgvsp: ENST00000562520.1:c.456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.456C>T
  hgvsp: ENST00000563137.2:c.456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.285C>T
  hgvsp: ENST00000535559.1:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.285C>T
  hgvsp: ENST00000567169.1:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.636C>T
  hgvsp: ENST00000561648.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.636C>T
  hgvsp: ENST00000262383.2:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22163
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4045
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3878
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3693
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 3.75e1
  variant carriers: 0
hgvs: p.His212His
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

16-49672430-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672430
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672430
    reference: chr 16
allele count: 1
allele frequency: 8.348778573694668e-6
allele num: 119778
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.453C>A
  hgvsp: ENST00000562520.1:c.453C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.633C>A
  hgvsp: ENST00000561648.1:c.633C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.282C>A
  hgvsp: ENST00000567169.1:c.282C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.633C>A
  hgvsp: ENST00000262383.2:c.633C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.453C>A
  hgvsp: ENST00000563137.2:c.453C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.282C>A
  hgvsp: ENST00000535559.1:c.282C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.453C>A
  hgvsp: ENST00000562871.1:c.453C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4044
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17991
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22152
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1148
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3875
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile211Ile
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/16-49672433-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672433
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672433
    reference: chr 16
allele count: 1
allele frequency: 8.347106058329577e-6
allele num: 119802
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.450G>T
  hgvsp: ENSP00000455588.2:p.Lys150Asn
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.630G>T
  hgvsp: ENSP00000262383.2:p.Lys210Asn
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.450G>T
  hgvsp: ENSP00000457664.1:p.Lys150Asn
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.630G>T
  hgvsp: ENSP00000455426.1:p.Lys210Asn
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.279G>T
  hgvsp: ENSP00000455061.1:p.Lys93Asn
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.279G>T
  hgvsp: ENSP00000442321.1:p.Lys93Asn
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.450G>T
  hgvsp: ENSP00000457928.1:p.Lys150Asn
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22164
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17985
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1147
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3099
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Lys210Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff

16-49672436-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672436
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672436
    reference: chr 16
allele count: 1
allele frequency: 8.34599142032082e-6
allele num: 119818
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.627C>T
  hgvsp: ENST00000262383.2:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.447C>T
  hgvsp: ENST00000563137.2:c.447C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.447C>T
  hgvsp: ENST00000562520.1:c.447C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.627C>T
  hgvsp: ENST00000561648.1:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.276C>T
  hgvsp: ENST00000535559.1:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.447C>T
  hgvsp: ENST00000562871.1:c.447C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.276C>T
  hgvsp: ENST00000567169.1:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10451
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17983
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4047
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2282
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33694
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1116
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3686
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1120
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu209Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

16-49672445-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672445
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672445
    reference: chr 16
allele count: 2
allele frequency: 1.667055646317474e-5
allele num: 119972
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.438C>T
  hgvsp: ENST00000562871.1:c.438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.438C>T
  hgvsp: ENST00000563137.2:c.438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.267C>T
  hgvsp: ENST00000535559.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.618C>T
  hgvsp: ENST00000561648.1:c.618C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.438C>T
  hgvsp: ENST00000562520.1:c.438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.618C>T
  hgvsp: ENST00000262383.2:c.618C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.267C>T
  hgvsp: ENST00000567169.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4057
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10495
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3698
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3889
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1116
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1150
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser206Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

16-49672450-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672450
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672450
    reference: chr 16
allele count: 1
allele frequency: 8.325701440346349e-6
allele num: 120110
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.262C>T
  hgvsp: ENSP00000455061.1:p.Arg88Cys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.433C>T
  hgvsp: ENSP00000457664.1:p.Arg145Cys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.262C>T
  hgvsp: ENSP00000442321.1:p.Arg88Cys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.613C>T
  hgvsp: ENSP00000262383.2:p.Arg205Cys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.433C>T
  hgvsp: ENSP00000457928.1:p.Arg145Cys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.613C>T
  hgvsp: ENSP00000455426.1:p.Arg205Cys
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.433C>T
  hgvsp: ENSP00000455588.2:p.Arg145Cys
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10526
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4063
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9420
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1119
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3901
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3103
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33965
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg205Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ

16-49672457-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 49672457
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 49672457
    reference: chr 16
allele count: 113
allele frequency: 9.395214260771239e-4
allele num: 120274
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455426
  ensembl transcript: ENST00000561648
  gene symbol: ZNF423
  hgvsc: ENST00000561648.1:c.606C>T
  hgvsp: ENST00000561648.1:c.606C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455588
  ensembl transcript: ENST00000563137
  gene symbol: ZNF423
  hgvsc: ENST00000563137.2:c.426C>T
  hgvsp: ENST00000563137.2:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000455061
  ensembl transcript: ENST00000567169
  gene symbol: ZNF423
  hgvsc: ENST00000567169.1:c.255C>T
  hgvsp: ENST00000567169.1:c.255C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000442321
  ensembl transcript: ENST00000535559
  gene symbol: ZNF423
  hgvsc: ENST00000535559.1:c.255C>T
  hgvsp: ENST00000535559.1:c.255C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000262383
  ensembl transcript: ENST00000262383
  gene symbol: ZNF423
  hgvsc: ENST00000262383.2:c.606C>T
  hgvsp: ENST00000262383.2:c.606C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457928
  ensembl transcript: ENST00000562871
  gene symbol: ZNF423
  hgvsc: ENST00000562871.1:c.426C>T
  hgvsp: ENST00000562871.1:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102935
  ensembl protein: ENSP00000457664
  ensembl transcript: ENST00000562520
  gene symbol: ZNF423
  hgvsc: ENST00000562520.1:c.426C>T
  hgvsp: ENST00000562520.1:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16762
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 18123
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22341
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4060
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 4.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 4.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala202Ala
num of homozygotes: 1
reference allele: G

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

GenotypeQuality
all individuals: 42
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2907
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2207
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1101
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3600
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9460
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3793
bin: 7.25e1
variant carriers: 0

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

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66590
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.62e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.97e-1

MQ
type: SiteQuality
SIO_000300: 5.907e1

FS
type: SiteQuality
SIO_000300: 2.559e0

MQRankSum
type: SiteQuality
SIO_000300: -2.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.123e0

QD
type: SiteQuality
SIO_000300: 9.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.700078e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.84e-1

GenotypeQuality
all individuals: 61
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3602
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1101
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9468
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3798
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2909
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2210
bin: 8.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66578
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.54e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

QD
type: SiteQuality
SIO_000300: 1.292e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.224e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e0

VQSLOD
type: SiteQuality
SIO_000300: 8.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.83e0

DP
type: SiteQuality
SIO_000300: 1.700391e6

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9463
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36079
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1082
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2912
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 34
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2209
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3598
bin: 7.75e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502087902184036e-5
allele num: 66574
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.925e1

VQSLOD
type: SiteQuality
SIO_000300: 3.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.57e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.98e-1

QD
type: SiteQuality
SIO_000300: 1.183e1

FS
type: SiteQuality
SIO_000300: 4.904e0

DP
type: SiteQuality
SIO_000300: 1.700411e6

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

GenotypeQuality
all individuals: 177
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3600
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1083
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2211
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3803
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501997656883655e-5
allele num: 66578
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.083e0

InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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VQSLOD
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QD
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BaseQRankSum
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SIO_000300: -1.703e0

DP
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SIO_000300: 1.700357e6

MQ
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SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: 1.45e0

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

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

East Asian
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allele frequency: 4.622140050843541e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.652048540189835e-4
allele num: 66584
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6580
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South Asian
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allele count: 2
allele frequency: 1.211387038158692e-4
allele num: 16510
num of homozygotes: 0

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

ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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DP
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QD
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MQ
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SIO_000300: 5.949e1

VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.003995313767311e-5
allele num: 66578
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Other
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VQSLOD
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QD
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MQ
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DP
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FS
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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SIO_000300: 3.99e-1

ClippingRankSum
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SIO_000300: -8.799999999999999e-2

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 1.501681883709755e-5
allele num: 66592
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
allele num: 8654
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Latino
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.056935190793458e-5
allele num: 16510
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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QD
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FS
type: SiteQuality
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MQRankSum
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DP
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BaseQRankSum
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SIO_000300: -2.92e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: -1.164e0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.00390507659958e-5
allele num: 66580
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 10398
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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Other
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ClippingRankSum
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SIO_000300: 1.82e-1

FS
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VQSLOD
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MQ
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MQRankSum
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BaseQRankSum
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QD
type: SiteQuality
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InbreedingCoeff
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DP
type: SiteQuality
SIO_000300: 1.700334e6

ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele num: 906
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66576
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African
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East Asian
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FS
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MQ
type: SiteQuality
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QD
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VQSLOD
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ReadPosRankSum
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DP
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

European (Finnish)
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allele frequency: 0.0e0
allele num: 6590
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66550
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African
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allele frequency: 0.0e0
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East Asian
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Other
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allele frequency: 0.0e0
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Latino
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QD
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MQRankSum
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MQ
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ClippingRankSum
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DP
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FS
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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East Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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Latino
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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FS
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DP
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MQRankSum
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MQ
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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Latino
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Other
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African
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European (Finnish)
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South Asian
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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DP
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QD
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BaseQRankSum
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ReadPosRankSum
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FS
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MQ
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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East Asian
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Other
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South Asian
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European (Non-Finnish)
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African
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VQSLOD
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DP
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InbreedingCoeff
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QD
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FS
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MQRankSum
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MQ
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1087
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3602
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66536
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.698788e6

MQRankSum
type: SiteQuality
SIO_000300: -5.669999999999999e-1

FS
type: SiteQuality
SIO_000300: 2.997e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.359e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.323e0

QD
type: SiteQuality
SIO_000300: 8.720000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.939e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.69e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.79e-1

GenotypeQuality
all individuals: 138
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 1087
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

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

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

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.730103806228374e-4
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66538
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.529e0

MQRankSum
type: SiteQuality
SIO_000300: 5.77e-1

DP
type: SiteQuality
SIO_000300: 1.698633e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.93e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

QD
type: SiteQuality
SIO_000300: 1.264e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.1e-1

GenotypeQuality
all individuals: 121
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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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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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
all individuals: 35470
bin: 6.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 7
allele frequency: 8.090614886731392e-4
allele num: 8652
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66518
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.79e-1

DP
type: SiteQuality
SIO_000300: 1.699176e6

MQRankSum
type: SiteQuality
SIO_000300: -3.24e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.91e-1

FS
type: SiteQuality
SIO_000300: 1.31e0

QD
type: SiteQuality
SIO_000300: 1.224e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
all individuals: 9413
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2931
bin: 9.75e1
variant carriers: 3

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.509108398965911e-5
allele num: 66532
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.179e0

DP
type: SiteQuality
SIO_000300: 1.699192e6

QD
type: SiteQuality
SIO_000300: 1.276e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.974e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.15e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.76e-1

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

GenotypeQuality
all individuals: 209
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3600
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variant carriers: 0

GenotypeQuality
all individuals: 140
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variant carriers: 0

GenotypeQuality
all individuals: 1107
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1087
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 5.25e1
variant carriers: 0

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
allele num: 6588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66496
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: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -3.491e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.698398e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.291e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.895e1

GenotypeQuality
all individuals: 3598
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2934
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 171
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1088
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2208
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.007699711260828e-5
allele num: 66496
num of homozygotes: 0

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
allele num: 6588
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: 8652
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 9.255000000000001e0

DP
type: SiteQuality
SIO_000300: 1.698591e6

QD
type: SiteQuality
SIO_000300: 1.376e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e0

VQSLOD
type: SiteQuality
SIO_000300: -1.461e-1

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2934
bin: 9.75e1
variant carriers: 1

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

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

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: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66496
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 6.61e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.461e-1

FS
type: SiteQuality
SIO_000300: 9.255000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

DP
type: SiteQuality
SIO_000300: 1.698591e6

QD
type: SiteQuality
SIO_000300: 1.376e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.97e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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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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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.008423586040914e-5
allele num: 66480
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.37e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

VQSLOD
type: SiteQuality
SIO_000300: 8.43e-1

QD
type: SiteQuality
SIO_000300: 1.512e1

DP
type: SiteQuality
SIO_000300: 1.698648e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.91e-1

FS
type: SiteQuality
SIO_000300: 4.605e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.19e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 1105
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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: 10382
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504121292341014e-5
allele num: 66484
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.69847e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e-2

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -4.5e-2

FS
type: SiteQuality
SIO_000300: 7.484e0

QD
type: SiteQuality
SIO_000300: 1.322e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.32e-1

GenotypeQuality
all individuals: 158
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 2.75e1
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GenotypeQuality
all individuals: 219
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GenotypeQuality
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GenotypeQuality
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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: 9370
bin: 6.75e1
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GenotypeQuality
all individuals: 1108
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50407604608489e-5
allele num: 66486
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -5.786e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.35e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.698192e6

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.08e-1

FS
type: SiteQuality
SIO_000300: 4.482e0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

European (Non-Finnish)
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allele count: 8
allele frequency: 1.203840250398772e-4
allele num: 66454
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8644
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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.56e-1

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -2.7e-2

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.967e1

FS
type: SiteQuality
SIO_000300: 1.119e0

DP
type: SiteQuality
SIO_000300: 1.698883e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.12e-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: 3

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.927153594141453e-4
allele num: 10378
num of homozygotes: 0

Latino
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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: 16510
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504528631179851e-5
allele num: 66466
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -4.99e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e0

DP
type: SiteQuality
SIO_000300: 1.698697e6

FS
type: SiteQuality
SIO_000300: 1.849e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

QD
type: SiteQuality
SIO_000300: 1.566e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.69e-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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66462
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.24e-1

DP
type: SiteQuality
SIO_000300: 1.69832e6

VQSLOD
type: SiteQuality
SIO_000300: 9.54e-1

FS
type: SiteQuality
SIO_000300: 2.909e0

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.886e0

QD
type: SiteQuality
SIO_000300: 1.041e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.951e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.096e0

GenotypeQuality
all individuals: 356
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 222
bin: 3.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504573904670197e-5
allele num: 66464
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
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: 1.077e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.367e0

VQSLOD
type: SiteQuality
SIO_000300: 6.23e-1

DP
type: SiteQuality
SIO_000300: 1.698373e6

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 3.626e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e0

GenotypeQuality
all individuals: 151
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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
all individuals: 2952
bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.927525057825752e-4
allele num: 10376
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66438
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.120000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.86e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.698772e6

MQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

QD
type: SiteQuality
SIO_000300: 1.206e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.55e-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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157407407407407e-4
allele num: 8640
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6594
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
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SIO_000300: 1.01e0

QD
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.17e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6592
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

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

South Asian
type: Population
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allele frequency: 0.0e0
allele num: 16508
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.009872381411028e-5
allele num: 66448
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Other
type: Population
allele count: 0
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allele num: 906
num of homozygotes: 0

African
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
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ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 5.913e1

ReadPosRankSum
type: SiteQuality
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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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: 1.506296318611797e-5
allele num: 66388
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European (Finnish)
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South Asian
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African
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BaseQRankSum
type: SiteQuality
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QD
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InbreedingCoeff
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MQRankSum
type: SiteQuality
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FS
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -9.04e-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
all individuals: 2964
bin: 9.75e1
variant carriers: 5

Latino
type: Population
allele count: 1
allele frequency: 8.655011251514626e-5
allele num: 11554
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66384
num of homozygotes: 0

European (Finnish)
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allele count: 0
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allele num: 6596
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South Asian
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allele count: 3
allele frequency: 1.817300702689605e-4
allele num: 16508
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157675387821255e-4
allele num: 8638
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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MQ
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QD
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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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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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1108
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66358
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.653513326410523e-5
allele num: 11556
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -4.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.517e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

FS
type: SiteQuality
SIO_000300: 5.245e0

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

VQSLOD
type: SiteQuality
SIO_000300: 3.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.700658e6

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

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3856
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507886245061673e-5
allele num: 66318
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.39e-1

DP
type: SiteQuality
SIO_000300: 1.700156e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.432e0

QD
type: SiteQuality
SIO_000300: 9.92e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.43e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.76e-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

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

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
allele num: 6602
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10308
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.016318281905107e-5
allele num: 66306
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.887e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.433e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.159999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.9e-2

FS
type: SiteQuality
SIO_000300: 1.086e0

VQSLOD
type: SiteQuality
SIO_000300: -3.54e-2

DP
type: SiteQuality
SIO_000300: 1.699903e6

QD
type: SiteQuality
SIO_000300: 1.209e1

GenotypeQuality
all individuals: 8
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66296
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.701202949165696e-5
allele num: 10308
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
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: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.85e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.4e-2

DP
type: SiteQuality
SIO_000300: 1.700101e6

QD
type: SiteQuality
SIO_000300: 1.053e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.07e0

FS
type: SiteQuality
SIO_000300: 1.391e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.46e-1

GenotypeQuality
all individuals: 180
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 34489
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GenotypeQuality
all individuals: 256
bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509479531457553e-5
allele num: 66248
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.38e-1

DP
type: SiteQuality
SIO_000300: 1.699507e6

FS
type: SiteQuality
SIO_000300: 1.177e0

MQRankSum
type: SiteQuality
SIO_000300: 8.139999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.28e-1

QD
type: SiteQuality
SIO_000300: 1.303e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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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
all individuals: 2974
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66246
num of homozygotes: 0

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

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
allele num: 6604
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: 8636
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 5.452562704471102e-4
allele num: 16506
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.79e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.16e-1

QD
type: SiteQuality
SIO_000300: 1.346e1

MQRankSum
type: SiteQuality
SIO_000300: 1.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.14e-1

DP
type: SiteQuality
SIO_000300: 1.699994e6

MQ
type: SiteQuality
SIO_000300: 5.938e1

GenotypeQuality
all individuals: 10
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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variant carriers: 85

GenotypeQuality
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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: 1
allele frequency: 9.725734292939116e-5
allele num: 10282
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 29
allele frequency: 4.387291981845689e-3
allele num: 6610
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 47
allele frequency: 7.097767978495273e-4
allele num: 66218
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.596952908587258e-4
allele num: 11552
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: 6
allele frequency: 3.63460140537921e-4
allele num: 16508
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.37e-1

QD
type: SiteQuality
SIO_000300: 1.391e1

FS
type: SiteQuality
SIO_000300: 1.096e0

VQSLOD
type: SiteQuality
SIO_000300: 4.14e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.399999999999999e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.87e-1

DP
type: SiteQuality
SIO_000300: 1.702115e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.42e-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
all individuals: 794
bin: 2.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
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: 11552
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512630464377553e-5
allele num: 66110
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.52e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.099e0

VQSLOD
type: SiteQuality
SIO_000300: -8.309e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.369999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.89e-1

FS
type: SiteQuality
SIO_000300: 5.021e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.6e0

DP
type: SiteQuality
SIO_000300: 1.697297e6

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: 30

African
type: Population
allele count: 26
allele frequency: 2.535595865028282e-3
allele num: 10254
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.731002250302925e-4
allele num: 11554
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512767759893501e-5
allele num: 66104
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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VQSLOD
type: SiteQuality
SIO_000300: 4.47e0

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.976e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

DP
type: SiteQuality
SIO_000300: 1.69823e6

FS
type: SiteQuality
SIO_000300: 5.17e-1

QD
type: SiteQuality
SIO_000300: 1.358e1

MQRankSum
type: SiteQuality
SIO_000300: 1.81e-1

GenotypeQuality
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bin: 9.25e1
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
all individuals: 192
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GenotypeQuality
all individuals: 3665
bin: 7.75e1
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GenotypeQuality
all individuals: 1107
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10246
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 6
allele frequency: 5.193905817174516e-4
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66098
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 2.512e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.047e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.68e-1

QD
type: SiteQuality
SIO_000300: 1.22e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.697337e6

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1109
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66050
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: 16508
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.782821365681862e-5
allele num: 10222
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.177e0

MQRankSum
type: SiteQuality
SIO_000300: -2.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.373e0

QD
type: SiteQuality
SIO_000300: 1.243e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.74e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.25e-1

DP
type: SiteQuality
SIO_000300: 1.694953e6

GenotypeQuality
all individuals: 9380
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 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
all individuals: 3666
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GenotypeQuality
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bin: 7.25e1
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: 10180
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: 1
allele frequency: 1.517128379403465e-5
allele num: 65914
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.66e-1

FS
type: SiteQuality
SIO_000300: 3.535e0

VQSLOD
type: SiteQuality
SIO_000300: -8.407e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.878e1

MQRankSum
type: SiteQuality
SIO_000300: -4.6e-2

QD
type: SiteQuality
SIO_000300: 1.496e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

DP
type: SiteQuality
SIO_000300: 1.691468e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.087e0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 1108
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 126
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variant carriers: 0

GenotypeQuality
all individuals: 2996
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variant carriers: 4

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.554148829583751e-5
allele num: 65874
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.658008658008658e-5
allele num: 11550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10152
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.39e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.9e-2

QD
type: SiteQuality
SIO_000300: 1.245e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.23e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

DP
type: SiteQuality
SIO_000300: 1.690951e6

GenotypeQuality
all individuals: 42
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1136
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2276
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1108
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3866
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2994
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9392
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variant carriers: 0

GenotypeQuality
all individuals: 3666
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34021
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
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: 11548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518556763651825e-5
allele num: 65852
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.83e-1

FS
type: SiteQuality
SIO_000300: 8.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.658e0

DP
type: SiteQuality
SIO_000300: 1.689951e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.35e-1

QD
type: SiteQuality
SIO_000300: 9.51e0

MQ
type: SiteQuality
SIO_000300: 5.887e1

GenotypeQuality
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1098
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variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
all individuals: 3869
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variant carriers: 0

GenotypeQuality
all individuals: 49
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GenotypeQuality
all individuals: 245
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GenotypeQuality
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GenotypeQuality
all individuals: 2995
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 105
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34050
bin: 6.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519018106695832e-5
allele num: 65832
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10136
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: 16508
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.99e-1

MQ
type: SiteQuality
SIO_000300: 5.988e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.31e-1

DP
type: SiteQuality
SIO_000300: 1.689595e6

QD
type: SiteQuality
SIO_000300: 1.385e1

VQSLOD
type: SiteQuality
SIO_000300: 9.09e-1

FS
type: SiteQuality
SIO_000300: 2.055e0

GenotypeQuality
all individuals: 275
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variant carriers: 0

GenotypeQuality
all individuals: 85
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 60
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variant carriers: 0

GenotypeQuality
all individuals: 1136
bin: 9.25e1
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GenotypeQuality
all individuals: 2995
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10120
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
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: 8632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519849230956289e-5
allele num: 65796
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.1e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

QD
type: SiteQuality
SIO_000300: 1.117e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

DP
type: SiteQuality
SIO_000300: 1.689021e6

MQRankSum
type: SiteQuality
SIO_000300: 3.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.14e0

VQSLOD
type: SiteQuality
SIO_000300: 5.16e-1

FS
type: SiteQuality
SIO_000300: 5.35e-1

GenotypeQuality
all individuals: 273
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 148
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 100
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GenotypeQuality
all individuals: 244
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10100
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521282745611099e-5
allele num: 65734
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.177e0

MQ
type: SiteQuality
SIO_000300: 5.921e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.554e0

VQSLOD
type: SiteQuality
SIO_000300: 6.900000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.18e-1

QD
type: SiteQuality
SIO_000300: 1.049e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.03e0

DP
type: SiteQuality
SIO_000300: 1.688268e6

GenotypeQuality
all individuals: 13
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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: 34003
bin: 6.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521792062332603e-5
allele num: 65712
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10092
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.39e-1

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.687742e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.61e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 259
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3683
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GenotypeQuality
all individuals: 1110
bin: 8.75e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.158480074142725e-4
allele num: 8632
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10064
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65674
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.686828e6

VQSLOD
type: SiteQuality
SIO_000300: -5.281e-1

FS
type: SiteQuality
SIO_000300: 4.866e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e0

QD
type: SiteQuality
SIO_000300: 1.067e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.752e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

GenotypeQuality
all individuals: 58
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
all individuals: 1159
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3875
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1111
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10058
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
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: 1.523043650431021e-5
allele num: 65658
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.85e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.72e-1

FS
type: SiteQuality
SIO_000300: 8.33e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.42e0

DP
type: SiteQuality
SIO_000300: 1.686585e6

QD
type: SiteQuality
SIO_000300: 1.191e1

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3871
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 3.75e1
variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 1.991635132443736e-4
allele num: 10042
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: 65626
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.43e0

DP
type: SiteQuality
SIO_000300: 1.686153e6

MQRankSum
type: SiteQuality
SIO_000300: -5.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.6e-2

QD
type: SiteQuality
SIO_000300: 1.164e1

FS
type: SiteQuality
SIO_000300: 6.825e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.56e-1

GenotypeQuality
all individuals: 97
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3675
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
all individuals: 1111
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2997
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variant carriers: 1

GenotypeQuality
all individuals: 9381
bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52494815176284e-5
allele num: 65576
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10000
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.977e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.01e-1

QD
type: SiteQuality
SIO_000300: 1.441e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.034e0

DP
type: SiteQuality
SIO_000300: 1.685415e6

VQSLOD
type: SiteQuality
SIO_000300: 3.39e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.73e-1

GenotypeQuality
all individuals: 83
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
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GenotypeQuality
all individuals: 2272
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variant carriers: 0

GenotypeQuality
all individuals: 75
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variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
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variant carriers: 0

GenotypeQuality
all individuals: 3871
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3671
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variant carriers: 0

GenotypeQuality
all individuals: 3001
bin: 9.75e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.57484445528852e-5
allele num: 65576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10014
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.964e1

FS
type: SiteQuality
SIO_000300: 1.655e0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

DP
type: SiteQuality
SIO_000300: 1.685223e6

BaseQRankSum
type: SiteQuality
SIO_000300: 8.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.12e-1

QD
type: SiteQuality
SIO_000300: 1.205e1

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.95e-1

GenotypeQuality
all individuals: 1164
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3878
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
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GenotypeQuality
all individuals: 99
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variant carriers: 0

GenotypeQuality
all individuals: 3001
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 3675
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1111
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1136
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 2.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.661008141347653e-5
allele num: 11546
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10010
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.5781955805152e-5
allele num: 65528
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.039e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 1.685552e6

MQRankSum
type: SiteQuality
SIO_000300: -4.0e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

QD
type: SiteQuality
SIO_000300: 8.050000000000001e0

GenotypeQuality
all individuals: 70
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9327
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
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variant carriers: 0

GenotypeQuality
all individuals: 1179
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 82
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GenotypeQuality
all individuals: 3644
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GenotypeQuality
all individuals: 3262
bin: 9.75e1
variant carriers: 285

GenotypeQuality
all individuals: 1126
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
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variant carriers: 1

GenotypeQuality
all individuals: 33669
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 263
allele frequency: 2.626323147593369e-2
allele num: 10014
num of homozygotes: 4

Latino
type: Population
allele count: 20
allele frequency: 1.732501732501732e-3
allele num: 11544
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 4.454342984409799e-3
allele num: 898
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.212121212121212e-4
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.051385328939338e-5
allele num: 65544
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.69783e6

QD
type: SiteQuality
SIO_000300: 1.353e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.97e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.34e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.32e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.02e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.27e-1

FS
type: SiteQuality
SIO_000300: 5.22e-1

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9346
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
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variant carriers: 0

GenotypeQuality
all individuals: 51
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GenotypeQuality
all individuals: 3669
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GenotypeQuality
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GenotypeQuality
all individuals: 3091
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 285
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variant carriers: 0

GenotypeQuality
all individuals: 2280
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variant carriers: 0

GenotypeQuality
all individuals: 3875
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GenotypeQuality
all individuals: 267
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10024
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 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: 11546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65498
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.983e1

MQRankSum
type: SiteQuality
SIO_000300: 4.46e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.429e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.069e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.853e0

VQSLOD
type: SiteQuality
SIO_000300: 2.05e0

DP
type: SiteQuality
SIO_000300: 1.689589e6

GenotypeQuality
all individuals: 77
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1116
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 84
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GenotypeQuality
all individuals: 32
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
all individuals: 3092
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GenotypeQuality
all individuals: 9354
bin: 6.75e1
variant carriers: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10026
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526437904506045e-5
allele num: 65512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.9e-1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.127e1

FS
type: SiteQuality
SIO_000300: 9.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e-1

MQ
type: SiteQuality
SIO_000300: 5.793e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

DP
type: SiteQuality
SIO_000300: 1.6897e6

GenotypeQuality
all individuals: 1171
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1137
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 56
bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 38
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GenotypeQuality
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GenotypeQuality
all individuals: 3667
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variant carriers: 0

GenotypeQuality
all individuals: 3878
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10008
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526437904506045e-5
allele num: 65512
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.096e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

FS
type: SiteQuality
SIO_000300: 1.829e0

MQRankSum
type: SiteQuality
SIO_000300: -6.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

VQSLOD
type: SiteQuality
SIO_000300: -1.034e0

MQ
type: SiteQuality
SIO_000300: 5.753e1

DP
type: SiteQuality
SIO_000300: 1.689813e6

GenotypeQuality
all individuals: 273
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1137
bin: 2.25e1
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GenotypeQuality
all individuals: 9329
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variant carriers: 0

GenotypeQuality
all individuals: 1138
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33599
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3094
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65490
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9994
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

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

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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DP
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MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.268e0

ClippingRankSum
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SIO_000300: 1.06e0

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0.0e0
allele num: 8618
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65528
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10000
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Latino
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allele frequency: 8.662508662508663e-5
allele num: 11544
num of homozygotes: 0

MQRankSum
type: SiteQuality
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QD
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FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
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DP
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VQSLOD
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InbreedingCoeff
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MQ
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.46e-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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526391305675123e-5
allele num: 65514
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9998
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.121e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-1

InbreedingCoeff
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MQ
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VQSLOD
type: SiteQuality
SIO_000300: 8.0e-2

MQRankSum
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FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -5.620000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.89e-1

DP
type: SiteQuality
SIO_000300: 1.690014e6

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: 10002
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65510
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

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

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

South Asian
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allele count: 1
allele frequency: 6.062075654704171e-5
allele num: 16496
num of homozygotes: 0

MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
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VQSLOD
type: SiteQuality
SIO_000300: -1.382e-1

FS
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SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

QD
type: SiteQuality
SIO_000300: 1.291e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.57e-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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65540
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10012
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.664009703690868e-5
allele num: 11542
num of homozygotes: 0

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

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.962e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

QD
type: SiteQuality
SIO_000300: 7.93e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

DP
type: SiteQuality
SIO_000300: 1.690996e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.639999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.7e-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: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10030
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.062075654704171e-5
allele num: 16496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65574
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Other
type: Population
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allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

VQSLOD
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ClippingRankSum
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SIO_000300: 1.21e0

MQRankSum
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.3139e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

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

East Asian
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allele frequency: 0.0e0
allele num: 8618
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.524669146795145e-5
allele num: 65588
num of homozygotes: 0

South Asian
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.524250830716703e-5
allele num: 65606
num of homozygotes: 0

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

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

East Asian
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African
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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QD
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MQRankSum
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DP
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BaseQRankSum
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 8614
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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European (Finnish)
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African
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South Asian
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Other
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European (Non-Finnish)
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VQSLOD
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QD
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DP
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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FS
type: SiteQuality
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ReadPosRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 9409
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

Other
type: Population
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allele num: 900
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East Asian
type: Population
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.062075654704171e-5
allele num: 16496
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African
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allele frequency: 9.9147332936744e-5
allele num: 10086
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65736
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.973e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.21e0

MQRankSum
type: SiteQuality
SIO_000300: 2.02e-1

DP
type: SiteQuality
SIO_000300: 1.696757e6

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.2e-2

MQ
type: SiteQuality
SIO_000300: 5.943e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

QD
type: SiteQuality
SIO_000300: 7.36e0

GenotypeQuality
all individuals: 232
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 903
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2294
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1151
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3713
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519433555170632e-5
allele num: 65814
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10146
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.25e0

MQRankSum
type: SiteQuality
SIO_000300: -3.39e-1

QD
type: SiteQuality
SIO_000300: 1.162e1

VQSLOD
type: SiteQuality
SIO_000300: 9.379999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.53e-1

DP
type: SiteQuality
SIO_000300: 1.69975e6

FS
type: SiteQuality
SIO_000300: 1.072e0

MQ
type: SiteQuality
SIO_000300: 6.0e1