10-28884987-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28884987
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28884987
    reference: chr 10
allele count: 1
allele frequency: 8.478456242687331e-6
allele num: 117946
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.475+5226A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.610+5226A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.784+17A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*927+17A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.784+17A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.784+17A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.919+17A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.115+17A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.717+17A>G
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9922
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4119
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2115
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3284
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

10-28884992-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28884992
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28884992
    reference: chr 10
allele count: 2
allele frequency: 1.708817498291182e-5
allele num: 117040
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*927+22C>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.784+22C>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.475+5231C>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.717+22C>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.919+22C>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.784+22C>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.115+22C>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.784+22C>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.610+5231C>G
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17740
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17895
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1134
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

10-28884997-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28884997
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28884997
    reference: chr 10
allele count: 1
allele frequency: 8.603334652511313e-6
allele num: 116234
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.784+27C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*927+27C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.475+5236C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.717+27C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.610+5236C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.784+27C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.115+27C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.784+27C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.919+27C>T
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4996
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4192
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 987
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1132
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

10-28884998-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28884998
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28884998
    reference: chr 10
allele count: 7
allele frequency: 6.028142815314927e-5
allele num: 116122
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.115+28G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.475+5237G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.919+28G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.784+28G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.717+28G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.784+28G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*927+28G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.610+5237G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.784+28G>A
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17351
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9759
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5228
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1049
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3257
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

10-28885006-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28885006
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28885006
    reference: chr 10
allele count: 9
allele frequency: 7.858477550949129e-5
allele num: 114526
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.919+36A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.784+36A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.610+5245A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*927+36A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.475+5245A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.115+36A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.717+36A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.784+36A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.784+36A>G
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15601
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4835
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23121
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2707
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6295
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1473
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: A
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-28885008-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28885008
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28885008
    reference: chr 10
allele count: 1
allele frequency: 8.867763904653802e-6
allele num: 112768
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.717+38A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.610+5247A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.919+38A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*927+38A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.784+38A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.115+38A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.784+38A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.475+5247A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.784+38A>G
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13978
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7427
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5644
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5764
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2933
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2861
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1413
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6766
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

10-28885010-TTTCTAAGTTTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28885010
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28884999
    reference: chr 10
allele count: 7
allele frequency: 6.206664184000993e-5
allele num: 112782
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5637
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14128
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7403
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13041
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19512
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1118
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2382
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 656
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1244
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5875
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: TTTCTAAGTTTC
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

10-28885013-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28885013
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28885013
    reference: chr 10
allele count: 1
allele frequency: 8.866348660294717e-6
allele num: 112786
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.784+43C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.784+43C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.115+43C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.610+5252C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.475+5252C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.784+43C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.717+43C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.919+43C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*927+43C>T
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5625
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14198
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7368
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13086
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1243
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6080
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1140
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD

10-28885015-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28885015
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28885015
    reference: chr 10
allele count: 1
allele frequency: 8.902975374370115e-6
allele num: 112322
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*927+45A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.717+45A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.784+45A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.115+45A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.784+45A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.784+45A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.610+5254A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.475+5254A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.919+45A>G
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5446
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7334
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8185
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13461
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1475
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1996
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3710
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1118
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5796
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

10-28897064-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897064
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897064
    reference: chr 10
allele count: 2
allele frequency: 1.661626399920242e-5
allele num: 120364
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.116-51C>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.476-51C>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*928-51C>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.611-51C>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.920-51C>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.785-51C>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.785-51C>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.785-51C>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.718-51C>G
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30721
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11233
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1582
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42941
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

http://identifiers.org/exac.variant/10-28897066-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897066
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897066
    reference: chr 10
allele count: 1
allele frequency: 8.302613662781043e-6
allele num: 120444
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.116-49A>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.476-49A>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.785-49A>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.611-49A>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.920-49A>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*928-49A>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.718-49A>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.785-49A>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.785-49A>C
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11311
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

10-28897071-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897071
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897071
    reference: chr 10
allele count: 3
allele frequency: 2.48970920196521e-5
allele num: 120496
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*928-44T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.785-44T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.785-44T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.785-44T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.116-44T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.476-44T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.920-44T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.718-44T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.611-44T>C
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30821
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1580
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
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: T
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

10-28897081-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897081
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897081
    reference: chr 10
allele count: 1
allele frequency: 8.290086714307032e-6
allele num: 120626
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*928-34G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.116-34G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.920-34G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.785-34G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.785-34G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.785-34G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.611-34G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.476-34G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.718-34G>A
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1491
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

10-28897085-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897085
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897086
    reference: chr 10
allele count: 1
allele frequency: 8.284317786430287e-6
allele num: 120710
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.611-25dupT
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.718-25dupT
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.785-25dupT
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.920-25dupT
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.116-25dupT
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.785-25dupT
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*928-25dupT
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.785-25dupT
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.476-25dupT
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11304
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13313
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31296
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46220
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

10-28897087-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897087
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897087
    reference: chr 10
allele count: 4
allele frequency: 3.311971119611837e-5
allele num: 120774
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*928-28T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.785-28T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.718-28T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.116-28T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.785-28T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.611-28T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.920-28T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.785-28T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.476-28T>C
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11311
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1484
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1576
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

10-28897087-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897087
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897087
    reference: chr 10
allele count: 689
allele frequency: 5.704870253531389e-3
allele num: 120774
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.476-28T>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.920-28T>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.718-28T>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.116-28T>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.785-28T>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.785-28T>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.785-28T>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.611-28T>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*928-28T>G
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 4.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 31324
  bin: 2.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.75e1
  variant carriers: 381
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 11311
  bin: 3.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 13380
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 1597
  bin: 9.75e1
  variant carriers: 662
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7293
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.25e1
  variant carriers: 1
num of homozygotes: 23
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum

10-28897093-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897093
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897093
    reference: chr 10
allele count: 3
allele frequency: 2.481635894381576e-5
allele num: 120888
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.920-22G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*928-22G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.476-22G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.611-22G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.785-22G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.116-22G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.718-22G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.785-22G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.785-22G>A
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11512
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31834
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13670
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1508
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 703
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

10-28897101-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897101
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897101
    reference: chr 10
allele count: 5
allele frequency: 4.129091930102732e-5
allele num: 121092
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.785-14A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.476-14A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.718-14A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.611-14A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.920-14A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*928-14A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.116-14A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.785-14A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.785-14A>T
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11601
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13738
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47554
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

10-28897120-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897120
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897120
    reference: chr 10
allele count: 303
allele frequency: 2.49732135498228e-3
allele num: 121330
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.790A>G
  hgvsp: ENSP00000364816.3:p.Thr264Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.925A>G
  hgvsp: ENSP00000346986.4:p.Thr309Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.790A>G
  hgvsp: ENSP00000399706.1:p.Thr264Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.481A>G
  hgvsp: ENSP00000364797.1:p.Thr161Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.790A>G
  hgvsp: ENSP00000415727.1:p.Thr264Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.723A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.121A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*933A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.616A>G
  hgvsp: ENSP00000311106.4:p.Thr206Ala
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13795
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11649
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 32110
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 235
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1607
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr309Ala
num of homozygotes: 4
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/10-28897136-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897136
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897136
    reference: chr 10
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.739C>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.137C>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.806C>A
  hgvsp: ENSP00000364816.3:p.Pro269His
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.497C>A
  hgvsp: ENSP00000364797.1:p.Pro166His
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.632C>A
  hgvsp: ENSP00000311106.4:p.Pro211His
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.806C>A
  hgvsp: ENSP00000415727.1:p.Pro269His
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*949C>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.941C>A
  hgvsp: ENSP00000346986.4:p.Pro314His
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.806C>A
  hgvsp: ENSP00000399706.1:p.Pro269His
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11714
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48118
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro314His
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

10-28897137-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897137
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897137
    reference: chr 10
allele count: 4
allele frequency: 3.295164346321773e-5
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.807C>T
  hgvsp: ENST00000428935.1:c.807C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.942C>T
  hgvsp: ENST00000354911.4:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*950C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.807C>T
  hgvsp: ENST00000375664.4:c.807C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.498C>T
  hgvsp: ENST00000375646.1:c.498C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.807C>T
  hgvsp: ENST00000439676.1:c.807C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.740C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.633C>T
  hgvsp: ENST00000347934.4:c.633C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.138C>T
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1509
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro314Pro
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

10-28897138-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897138
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897138
    reference: chr 10
allele count: 4
allele frequency: 3.295164346321773e-5
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*951G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.741G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.943G>A
  hgvsp: ENSP00000346986.4:p.Val315Ile
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.634G>A
  hgvsp: ENSP00000311106.4:p.Val212Ile
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.808G>A
  hgvsp: ENSP00000364816.3:p.Val270Ile
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.808G>A
  hgvsp: ENSP00000415727.1:p.Val270Ile
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.808G>A
  hgvsp: ENSP00000399706.1:p.Val270Ile
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.139G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.499G>A
  hgvsp: ENSP00000364797.1:p.Val167Ile
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11719
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32294
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1507
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1617
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val315Ile
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

10-28897156-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897156
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897156
    reference: chr 10
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.826A>G
  hgvsp: ENSP00000415727.1:p.Thr276Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.759A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.652A>G
  hgvsp: ENSP00000311106.4:p.Thr218Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.961A>G
  hgvsp: ENSP00000346986.4:p.Thr321Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.517A>G
  hgvsp: ENSP00000364797.1:p.Thr173Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.826A>G
  hgvsp: ENSP00000364816.3:p.Thr276Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*969A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.157A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.826A>G
  hgvsp: ENSP00000399706.1:p.Thr276Ala
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11720
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32307
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1503
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr321Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/10-28897166-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897166
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897166
    reference: chr 10
allele count: 5
allele frequency: 4.11868399808893e-5
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.167C>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.971C>A
  hgvsp: ENSP00000346986.4:p.Thr324Lys
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.836C>A
  hgvsp: ENSP00000364816.3:p.Thr279Lys
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.527C>A
  hgvsp: ENSP00000364797.1:p.Thr176Lys
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*979C>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.836C>A
  hgvsp: ENSP00000415727.1:p.Thr279Lys
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.662C>A
  hgvsp: ENSP00000311106.4:p.Thr221Lys
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.769C>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.836C>A
  hgvsp: ENSP00000399706.1:p.Thr279Lys
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13852
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32308
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1611
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr324Lys
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: C
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD

10-28897166-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897166
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897166
    reference: chr 10
allele count: 2
allele frequency: 1.647473599235572e-5
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.836C>T
  hgvsp: ENSP00000399706.1:p.Thr279Met
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.769C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.662C>T
  hgvsp: ENSP00000311106.4:p.Thr221Met
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.167C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.836C>T
  hgvsp: ENSP00000364816.3:p.Thr279Met
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*979C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.527C>T
  hgvsp: ENSP00000364797.1:p.Thr176Met
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.836C>T
  hgvsp: ENSP00000415727.1:p.Thr279Met
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.971C>T
  hgvsp: ENSP00000346986.4:p.Thr324Met
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32308
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13852
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7536
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr324Met
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

10-28897176-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897176
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897176
    reference: chr 10
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.846C>T
  hgvsp: ENST00000439676.1:c.846C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.846C>T
  hgvsp: ENST00000428935.1:c.846C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*989C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.779C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.981C>T
  hgvsp: ENST00000354911.4:c.981C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.846C>T
  hgvsp: ENST00000375664.4:c.846C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.672C>T
  hgvsp: ENST00000347934.4:c.672C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.537C>T
  hgvsp: ENST00000375646.1:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.177C>T
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13849
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32310
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala327Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ

10-28897181-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897181
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897181
    reference: chr 10
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.784G>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.851G>C
  hgvsp: ENSP00000415727.1:p.Gly284Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.677G>C
  hgvsp: ENSP00000311106.4:p.Gly226Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.851G>C
  hgvsp: ENSP00000364816.3:p.Gly284Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.542G>C
  hgvsp: ENSP00000364797.1:p.Gly181Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.986G>C
  hgvsp: ENSP00000346986.4:p.Gly329Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.182G>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*994G>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.851G>C
  hgvsp: ENSP00000399706.1:p.Gly284Ala
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32315
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1498
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly329Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

10-28897191-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897191
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897191
    reference: chr 10
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.687C>G
  hgvsp: ENST00000347934.4:c.687C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.794C>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.192C>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.861C>G
  hgvsp: ENST00000375664.4:c.861C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.996C>G
  hgvsp: ENST00000354911.4:c.996C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.861C>G
  hgvsp: ENST00000428935.1:c.861C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1004C>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.552C>G
  hgvsp: ENST00000375646.1:c.552C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.861C>G
  hgvsp: ENST00000439676.1:c.861C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32314
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7541
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro332Pro
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

10-28897192-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897192
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897192
    reference: chr 10
allele count: 2
allele frequency: 1.64774506088418e-5
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.862A>G
  hgvsp: ENSP00000364816.3:p.Thr288Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.997A>G
  hgvsp: ENSP00000346986.4:p.Thr333Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.193A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.862A>G
  hgvsp: ENSP00000415727.1:p.Thr288Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.688A>G
  hgvsp: ENSP00000311106.4:p.Thr230Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.553A>G
  hgvsp: ENSP00000364797.1:p.Thr185Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.862A>G
  hgvsp: ENSP00000399706.1:p.Thr288Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.795A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1005A>G
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13840
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7540
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr333Ala
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

10-28897194-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897194
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897194
    reference: chr 10
allele count: 3
allele frequency: 2.471536142096851e-5
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1007A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.797A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.864A>T
  hgvsp: ENST00000439676.1:c.864A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.864A>T
  hgvsp: ENST00000428935.1:c.864A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.555A>T
  hgvsp: ENST00000375646.1:c.555A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.690A>T
  hgvsp: ENST00000347934.4:c.690A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.864A>T
  hgvsp: ENST00000375664.4:c.864A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.999A>T
  hgvsp: ENST00000354911.4:c.999A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.195A>T
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13839
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48152
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr333Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

10-28897207-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897207
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897207
    reference: chr 10
allele count: 4
allele frequency: 3.295815961636702e-5
allele num: 121366
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.568A>G
  hgvsp: ENSP00000364797.1:p.Thr190Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.208A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.877A>G
  hgvsp: ENSP00000364816.3:p.Thr293Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.877A>G
  hgvsp: ENSP00000415727.1:p.Thr293Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.877A>G
  hgvsp: ENSP00000399706.1:p.Thr293Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1012A>G
  hgvsp: ENSP00000346986.4:p.Thr338Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1020A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.810A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.703A>G
  hgvsp: ENSP00000311106.4:p.Thr235Ala
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32325
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13845
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48156
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 668
  bin: 9.75e1
  variant carriers: 4
hgvs: p.Thr338Ala
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP

10-28897207-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897207
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897207
    reference: chr 10
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.703A>T
  hgvsp: ENSP00000311106.4:p.Thr235Ser
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.877A>T
  hgvsp: ENSP00000399706.1:p.Thr293Ser
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.568A>T
  hgvsp: ENSP00000364797.1:p.Thr190Ser
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.810A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.208A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1012A>T
  hgvsp: ENSP00000346986.4:p.Thr338Ser
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.877A>T
  hgvsp: ENSP00000415727.1:p.Thr293Ser
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.877A>T
  hgvsp: ENSP00000364816.3:p.Thr293Ser
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1020A>T
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32325
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13845
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48156
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr338Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD

10-28897208-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897208
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897208
    reference: chr 10
allele count: 1
allele frequency: 8.239811473113496e-6
allele num: 121362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.704C>T
  hgvsp: ENSP00000311106.4:p.Thr235Ile
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.569C>T
  hgvsp: ENSP00000364797.1:p.Thr190Ile
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1013C>T
  hgvsp: ENSP00000346986.4:p.Thr338Ile
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.811C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.209C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.878C>T
  hgvsp: ENSP00000399706.1:p.Thr293Ile
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.878C>T
  hgvsp: ENSP00000415727.1:p.Thr293Ile
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.878C>T
  hgvsp: ENSP00000364816.3:p.Thr293Ile
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1021C>T
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13849
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1606
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48153
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr338Ile
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum

10-28897213-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897213
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897213
    reference: chr 10
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.883G>C
  hgvsp: ENSP00000364816.3:p.Ala295Pro
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.883G>C
  hgvsp: ENSP00000415727.1:p.Ala295Pro
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.816G>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.883G>C
  hgvsp: ENSP00000399706.1:p.Ala295Pro
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1026G>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1018G>C
  hgvsp: ENSP00000346986.4:p.Ala340Pro
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.574G>C
  hgvsp: ENSP00000364797.1:p.Ala192Pro
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.709G>C
  hgvsp: ENSP00000311106.4:p.Ala237Pro
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.214G>C
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala340Pro
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

10-28897217-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897217
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897217
    reference: chr 10
allele count: 2
allele frequency: 1.647907980818351e-5
allele num: 121366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.713C>T
  hgvsp: ENSP00000311106.4:p.Ser238Leu
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1030C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.820C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.887C>T
  hgvsp: ENSP00000364816.3:p.Ser296Leu
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.887C>T
  hgvsp: ENSP00000399706.1:p.Ser296Leu
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1022C>T
  hgvsp: ENSP00000346986.4:p.Ser341Leu
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.218C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.887C>T
  hgvsp: ENSP00000415727.1:p.Ser296Leu
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.578C>T
  hgvsp: ENSP00000364797.1:p.Ser193Leu
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11716
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13854
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7531
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser341Leu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

10-28897220-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897220
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897220
    reference: chr 10
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1033C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.716C>T
  hgvsp: ENSP00000311106.4:p.Ala239Val
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.890C>T
  hgvsp: ENSP00000415727.1:p.Ala297Val
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.581C>T
  hgvsp: ENSP00000364797.1:p.Ala194Val
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.221C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.890C>T
  hgvsp: ENSP00000399706.1:p.Ala297Val
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1025C>T
  hgvsp: ENSP00000346986.4:p.Ala342Val
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.823C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.890C>T
  hgvsp: ENSP00000364816.3:p.Ala297Val
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13849
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala342Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum

10-28897221-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897221
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897221
    reference: chr 10
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.891G>A
  hgvsp: ENST00000428935.1:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.222G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.891G>A
  hgvsp: ENST00000375664.4:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1026G>A
  hgvsp: ENST00000354911.4:c.1026G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.824G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.891G>A
  hgvsp: ENST00000439676.1:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.717G>A
  hgvsp: ENST00000347934.4:c.717G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.582G>A
  hgvsp: ENST00000375646.1:c.582G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1034G>A
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13849
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11716
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala342Ala
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

10-28897227-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897227
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897227
    reference: chr 10
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.897T>A
  hgvsp: ENST00000439676.1:c.897T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.830T>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.588T>A
  hgvsp: ENST00000375646.1:c.588T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.897T>A
  hgvsp: ENST00000375664.4:c.897T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.228T>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.723T>A
  hgvsp: ENST00000347934.4:c.723T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.897T>A
  hgvsp: ENST00000428935.1:c.897T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1032T>A
  hgvsp: ENST00000354911.4:c.1032T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1040T>A
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32336
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11704
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1603
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7514
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro344Pro
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ

10-28897227-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897227
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897227
    reference: chr 10
allele count: 2
allele frequency: 1.648614339647526e-5
allele num: 121314
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.897T>C
  hgvsp: ENST00000439676.1:c.897T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.588T>C
  hgvsp: ENST00000375646.1:c.588T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.228T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.897T>C
  hgvsp: ENST00000375664.4:c.897T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.897T>C
  hgvsp: ENST00000428935.1:c.897T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.830T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.723T>C
  hgvsp: ENST00000347934.4:c.723T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1040T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1032T>C
  hgvsp: ENST00000354911.4:c.1032T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32336
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11704
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1603
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro344Pro
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP

10-28897234-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897234
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897234
    reference: chr 10
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.904C>T
  hgvsp: ENSP00000364816.3:p.Pro302Ser
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1039C>T
  hgvsp: ENSP00000346986.4:p.Pro347Ser
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.904C>T
  hgvsp: ENSP00000399706.1:p.Pro302Ser
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.595C>T
  hgvsp: ENSP00000364797.1:p.Pro199Ser
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.730C>T
  hgvsp: ENSP00000311106.4:p.Pro244Ser
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.904C>T
  hgvsp: ENSP00000415727.1:p.Pro302Ser
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1047C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.235C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.837C>T
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13844
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32343
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro347Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

10-28897240-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897240
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897240
    reference: chr 10
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.843C>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.736C>G
  hgvsp: ENSP00000311106.4:p.Pro246Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.910C>G
  hgvsp: ENSP00000364816.3:p.Pro304Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1053C>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.601C>G
  hgvsp: ENSP00000364797.1:p.Pro201Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1045C>G
  hgvsp: ENSP00000346986.4:p.Pro349Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.910C>G
  hgvsp: ENSP00000415727.1:p.Pro304Ala
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.241C>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.910C>G
  hgvsp: ENSP00000399706.1:p.Pro304Ala
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11666
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro349Ala
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

10-28897247-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897247
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897247
    reference: chr 10
allele count: 6
allele frequency: 4.95074013565028e-5
allele num: 121194
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.608C>T
  hgvsp: ENSP00000364797.1:p.Ser203Leu
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.917C>T
  hgvsp: ENSP00000364816.3:p.Ser306Leu
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.850C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.917C>T
  hgvsp: ENSP00000415727.1:p.Ser306Leu
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1060C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1052C>T
  hgvsp: ENSP00000346986.4:p.Ser351Leu
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.743C>T
  hgvsp: ENSP00000311106.4:p.Ser248Leu
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.248C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.917C>T
  hgvsp: ENSP00000399706.1:p.Ser306Leu
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32286
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13878
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser351Leu
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: C
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

10-28897248-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897248
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897248
    reference: chr 10
allele count: 2
allele frequency: 1.651173158529135e-5
allele num: 121126
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1053G>A
  hgvsp: ENST00000354911.4:c.1053G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.918G>A
  hgvsp: ENST00000375664.4:c.918G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.851G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.918G>A
  hgvsp: ENST00000439676.1:c.918G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.744G>A
  hgvsp: ENST00000347934.4:c.744G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.609G>A
  hgvsp: ENST00000375646.1:c.609G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.249G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1061G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.918G>A
  hgvsp: ENST00000428935.1:c.918G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11617
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13886
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32291
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 655
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 48062
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser351Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

10-28897248-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897248
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897248
    reference: chr 10
allele count: 1
allele frequency: 8.255865792645674e-6
allele num: 121126
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.918G>T
  hgvsp: ENST00000428935.1:c.918G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.851G>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.918G>T
  hgvsp: ENST00000439676.1:c.918G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.249G>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.918G>T
  hgvsp: ENST00000375664.4:c.918G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1061G>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.744G>T
  hgvsp: ENST00000347934.4:c.744G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.609G>T
  hgvsp: ENST00000375646.1:c.609G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1053G>T
  hgvsp: ENST00000354911.4:c.1053G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11617
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32291
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13886
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 655
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser351Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/10-28897276-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897276
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897276
    reference: chr 10
allele count: 1
allele frequency: 8.368060785593547e-6
allele num: 119502
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1081A>C
  hgvsp: ENSP00000346986.4:p.Asn361His
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.946A>C
  hgvsp: ENSP00000415727.1:p.Asn316His
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.637A>C
  hgvsp: ENSP00000364797.1:p.Asn213His
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.946A>C
  hgvsp: ENSP00000399706.1:p.Asn316His
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.2A>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.879A>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.772A>C
  hgvsp: ENSP00000311106.4:p.Asn258His
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.946A>C
  hgvsp: ENSP00000364816.3:p.Asn316His
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1089A>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.277A>C
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10775
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14151
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn361His
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD

10-28897276-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897276
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897276
    reference: chr 10
allele count: 2
allele frequency: 1.673612157118709e-5
allele num: 119502
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.637A>G
  hgvsp: ENSP00000364797.1:p.Asn213Asp
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.2A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1081A>G
  hgvsp: ENSP00000346986.4:p.Asn361Asp
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1089A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.772A>G
  hgvsp: ENSP00000311106.4:p.Asn258Asp
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.277A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.946A>G
  hgvsp: ENSP00000399706.1:p.Asn316Asp
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.946A>G
  hgvsp: ENSP00000364816.3:p.Asn316Asp
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.879A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.946A>G
  hgvsp: ENSP00000415727.1:p.Asn316Asp
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10775
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14151
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1845
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn361Asp
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

10-28897286-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897286
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897286
    reference: chr 10
allele count: 3
allele frequency: 2.557239545152326e-5
allele num: 117314
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.956G>A
  hgvsp: ENSP00000364816.3:p.Arg319Lys
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.956G>A
  hgvsp: ENSP00000399706.1:p.Arg319Lys
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.647G>A
  hgvsp: ENSP00000364797.1:p.Arg216Lys
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1091G>A
  hgvsp: ENSP00000346986.4:p.Arg364Lys
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.287G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.12G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.782G>A
  hgvsp: ENSP00000311106.4:p.Arg261Lys
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.956G>A
  hgvsp: ENSP00000415727.1:p.Arg319Lys
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.889G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1099G>A
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29775
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13904
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1253
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 5.75e1
  variant carriers: 1
hgvs: p.Arg364Lys
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

10-28897287-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897287
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897287
    reference: chr 10
allele count: 1
allele frequency: 8.556955093099671e-6
allele num: 116864
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.957A>G
  hgvsp: ENST00000439676.1:c.957A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.957A>G
  hgvsp: ENST00000428935.1:c.957A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.957A>G
  hgvsp: ENST00000375664.4:c.957A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.783A>G
  hgvsp: ENST00000347934.4:c.783A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.890A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.648A>G
  hgvsp: ENST00000375646.1:c.648A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1092A>G
  hgvsp: ENST00000354911.4:c.1092A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.288A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.13A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1100A>G
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10013
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13830
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg364Arg
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ

10-28897290-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897290
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897290
    reference: chr 10
allele count: 1
allele frequency: 8.651117724409994e-6
allele num: 115592
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1103A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.16A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.960A>G
  hgvsp: ENST00000428935.1:c.960A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.291A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.786A>G
  hgvsp: ENST00000347934.4:c.786A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.960A>G
  hgvsp: ENST00000375664.4:c.960A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1095A>G
  hgvsp: ENST00000354911.4:c.1095A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.651A>G
  hgvsp: ENST00000375646.1:c.651A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.893A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.960A>G
  hgvsp: ENST00000439676.1:c.960A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9653
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28610
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13727
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1003
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gln365Gln
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

10-28897314-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897314
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897314
    reference: chr 10
allele count: 9
allele frequency: 9.470693465221509e-5
allele num: 95030
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.984G>A
  hgvsp: ENST00000428935.1:c.984G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1119G>A
  hgvsp: ENST00000354911.4:c.1119G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.315G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.675G>A
  hgvsp: ENST00000375646.1:c.675G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.984G>A
  hgvsp: ENST00000375664.4:c.984G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.810G>A
  hgvsp: ENST00000347934.4:c.810G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.40G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.917G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1127G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.984G>A
  hgvsp: ENST00000439676.1:c.984G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12934
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12010
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16094
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11014
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26014
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr373Thr
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

10-28897336-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897336
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897336
    reference: chr 10
allele count: 2
allele frequency: 2.699856907583898e-5
allele num: 74078
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.697G>A
  hgvsp: ENSP00000364797.1:p.Val233Met
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.62G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.337G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1141G>A
  hgvsp: ENSP00000346986.4:p.Val381Met
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.1006G>A
  hgvsp: ENSP00000415727.1:p.Val336Met
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1149G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.1006G>A
  hgvsp: ENSP00000364816.3:p.Val336Met
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.832G>A
  hgvsp: ENSP00000311106.4:p.Val278Met
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.1006G>A
  hgvsp: ENSP00000399706.1:p.Val336Met
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.939G>A
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6829
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6483
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18534
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1512
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val381Met
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

10-28897351-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897351
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897351
    reference: chr 10
allele count: 1
allele frequency: 1.703519471227556e-5
allele num: 58702
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1156A>G
  hgvsp: ENSP00000346986.4:p.Ile386Val
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.1021A>G
  hgvsp: ENSP00000415727.1:p.Ile341Val
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.352A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1164A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.1021A>G
  hgvsp: ENSP00000364816.3:p.Ile341Val
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.954A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.1021A>G
  hgvsp: ENSP00000399706.1:p.Ile341Val
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.847A>G
  hgvsp: ENSP00000311106.4:p.Ile283Val
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.712A>G
  hgvsp: ENSP00000364797.1:p.Ile238Val
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.77A>G
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19322
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16876
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4929
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ile386Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

10-28897356-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897356
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897356
    reference: chr 10
allele count: 2
allele frequency: 3.965264284864586e-5
allele num: 50438
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.1026T>C
  hgvsp: ENST00000439676.1:c.1026T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.717T>C
  hgvsp: ENST00000375646.1:c.717T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.959T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.852T>C
  hgvsp: ENST00000347934.4:c.852T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1169T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.1026T>C
  hgvsp: ENST00000428935.1:c.1026T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.1026T>C
  hgvsp: ENST00000375664.4:c.1026T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.82T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1161T>C
  hgvsp: ENST00000354911.4:c.1161T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.357T>C
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14933
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4477
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14375
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1350
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asn387Asn
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

10-28897369-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897369
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897369
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 33272
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.370T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.86+9T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.1030+9T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.1030+9T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1173+9T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.721+9T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.963+9T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1165+9T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.1030+9T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.856+9T>C
  variant of: http://identifiers.org/hgnc/17327
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25321
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15715
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9009
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1709
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

10-28897371-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897371
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897371
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 32036
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.1030+11A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.856+11A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.721+11A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.86+11A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.1030+11A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.372A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1173+11A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.1030+11A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1165+11A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.963+11A>G
  variant of: http://identifiers.org/hgnc/17327
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26097
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15414
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8632
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1483
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ

10-28897391-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897391
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897391
    reference: chr 10
allele count: 2
allele frequency: 9.77421561919656e-5
allele num: 20462
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1173+31T>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.1030+31T>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.856+31T>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.1030+31T>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1165+31T>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.392T>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.721+31T>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.963+31T>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.1030+31T>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.86+31T>G
  variant of: http://identifiers.org/hgnc/17327
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5640
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11107
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32222
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1188
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1511
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

10-28897397-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897397
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897397
    reference: chr 10
allele count: 1
allele frequency: 5.364806866952789e-5
allele num: 18640
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.1030+37C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.721+37C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.1030+37C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1165+37C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.1030+37C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.398C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1173+37C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.963+37C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.86+37C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.856+37C>T
  variant of: http://identifiers.org/hgnc/17327
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10794
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32222
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4951
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1159
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28695
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/10-28897404-CAA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897404
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897402
    reference: chr 10
allele count: 1
allele frequency: 5.847953216374269e-5
allele num: 17100
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.856+46_856+47delAA
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.721+46_721+47delAA
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.86+46_86+47delAA
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.1030+46_1030+47delAA
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1173+46_*1173+47delAA
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.1030+46_1030+47delAA
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.1030+46_1030+47delAA
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1165+46_1165+47delAA
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.963+46_963+47delAA
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.407_408delAA
  variant of: http://identifiers.org/hgnc/17327
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11041
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31925
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4404
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1110
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 908
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: CAA
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

10-28897409-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897409
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897409
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 16370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.1030+49T>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1173+49T>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.721+49T>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.410T>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.963+49T>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1165+49T>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.1030+49T>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.856+49T>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.86+49T>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.1030+49T>A
  variant of: http://identifiers.org/hgnc/17327
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31909
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11178
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24515
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

10-28897412-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28897412
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28897412
    reference: chr 10
allele count: 2
allele frequency: 1.249375312343828e-4
allele num: 16008
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.721+52T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.963+52T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.86+52T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1165+52T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.1030+52T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.856+52T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.1030+52T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.1030+52T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000476046
  gene symbol: WAC
  hgvsc: ENST00000476046.1:n.413T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1173+52T>C
  variant of: http://identifiers.org/hgnc/17327
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31939
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11190
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1485
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/10-28899580-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28899580
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28899580
    reference: chr 10
allele count: 7
allele frequency: 5.89255349596781e-5
allele num: 118794
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.87-48C>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.1031-48C>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1166-48C>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.1031-48C>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.722-60C>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.964-57C>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1174-48C>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.857-48C>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.1031-48C>A
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6481
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4726
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5982
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6083
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3347
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1021
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP

10-28899580-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28899580
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28899580
    reference: chr 10
allele count: 3
allele frequency: 2.52538006970049e-5
allele num: 118794
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.1031-48C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1174-48C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.964-57C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.857-48C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.87-48C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.1031-48C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1166-48C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.1031-48C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.722-60C>T
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4726
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6083
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6481
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5982
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3347
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1055
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1710
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

10-28899581-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28899581
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28899581
    reference: chr 10
allele count: 2
allele frequency: 1.680672268907563e-5
allele num: 119000
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.1031-47A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.1031-47A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1166-47A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.1031-47A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.857-47A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.964-56A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.722-59A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.87-47A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1174-47A>T
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6084
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4726
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5982
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6481
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3184
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1050
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 640
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 796
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1859
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

10-28899585-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28899585
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28899585
    reference: chr 10
allele count: 5
allele frequency: 4.200409960012097e-5
allele num: 119036
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.722-55G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.857-43G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.1031-43G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.87-43G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1166-43G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.964-52G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.1031-43G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.1031-43G>A
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1174-43G>A
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6091
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5987
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3347
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1307
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1092
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

10-28899589-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28899589
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28899589
    reference: chr 10
allele count: 1
allele frequency: 8.390810384466932e-6
allele num: 119178
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.1031-39C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.1031-39C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.964-48C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1174-39C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.87-39C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.1031-39C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.722-51C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1166-39C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.857-39C>T
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6094
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6481
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3229
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5986
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 658
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1006
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1069
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

10-28899594-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28899594
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28899594
    reference: chr 10
allele count: 1
allele frequency: 8.38321345338095e-6
allele num: 119286
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.857-34T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1174-34T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.1031-34T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1166-34T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.964-43T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.1031-34T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.1031-34T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.87-34T>C
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.722-46T>C
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6095
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5987
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3249
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4728
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 973
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 926
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

10-28899600-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28899600
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28899600
    reference: chr 10
allele count: 1
allele frequency: 8.373245805003851e-6
allele num: 119428
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.1031-28A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.87-28A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1174-28A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.1031-28A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.964-37A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.722-40A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.857-28A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.1031-28A>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1166-28A>T
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5987
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1000
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 668
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

10-28899602-GAAT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28899602
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28899599
    reference: chr 10
allele count: 1
allele frequency: 8.369041242635244e-6
allele num: 119488
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1174-25_*1174-23delAAT
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.964-34_964-32delAAT
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.857-25_857-23delAAT
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1166-25_1166-23delAAT
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.87-25_87-23delAAT
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.722-37_722-35delAAT
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.1031-25_1031-23delAAT
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.1031-25_1031-23delAAT
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.1031-25_1031-23delAAT
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5987
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4218
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4735
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4423
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: GAAT
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ

10-28899608-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28899608
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28899608
    reference: chr 10
allele count: 2
allele frequency: 1.668362835549475e-5
allele num: 119878
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.722-32A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1166-20A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000404125
  ensembl transcript: ENST00000424454
  gene symbol: WAC
  hgvsc: ENST00000424454.1:c.*1174-20A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.1031-20A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.1031-20A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.87-20A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.857-20A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.1031-20A>G
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.964-29A>G
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5987
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4741
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4171
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1325
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1095
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

10-28899646-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28899646
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 28899646
    reference: chr 10
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000415727
  ensembl transcript: ENST00000439676
  gene symbol: WAC
  hgvsc: ENST00000439676.1:c.1049C>T
  hgvsp: ENSP00000415727.1:p.Thr350Ile
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000345541
  gene symbol: WAC
  hgvsc: ENST00000345541.6:n.973C>T
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364797
  ensembl transcript: ENST00000375646
  gene symbol: WAC
  hgvsc: ENST00000375646.1:c.728C>T
  hgvsp: ENSP00000364797.1:p.Thr243Ile
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000364816
  ensembl transcript: ENST00000375664
  gene symbol: WAC
  hgvsc: ENST00000375664.4:c.1049C>T
  hgvsp: ENSP00000364816.3:p.Thr350Ile
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000399706
  ensembl transcript: ENST00000428935
  gene symbol: WAC
  hgvsc: ENST00000428935.1:c.1049C>T
  hgvsp: ENSP00000399706.1:p.Thr350Ile
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000311106
  ensembl transcript: ENST00000347934
  gene symbol: WAC
  hgvsc: ENST00000347934.4:c.875C>T
  hgvsp: ENSP00000311106.4:p.Thr292Ile
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095787
  ensembl protein: ENSP00000346986
  ensembl transcript: ENST00000354911
  gene symbol: WAC
  hgvsc: ENST00000354911.4:c.1184C>T
  hgvsp: ENSP00000346986.4:p.Thr395Ile
  variant of: http://identifiers.org/hgnc/17327
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000095787
  ensembl transcript: ENST00000495268
  gene symbol: WAC
  hgvsc: ENST00000495268.2:n.105C>T
  variant of: http://identifiers.org/hgnc/17327
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5987
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr395Ile
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 9114
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4195
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 57
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31291
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 843
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1135
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2832
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14552
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10280
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
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: 880
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.42e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.678e0

MQ
type: SiteQuality
SIO_000300: 5.896e1

DP
type: SiteQuality
SIO_000300: 1.685945e6

VQSLOD
type: SiteQuality
SIO_000300: -1.295e0

QD
type: SiteQuality
SIO_000300: 1.114e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.031e0

GenotypeQuality
all individuals: 89
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8937
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4195
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2113
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2808
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.419244961680386e-4
allele num: 14092
num of homozygotes: 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: 10236
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65184
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

DP
type: SiteQuality
SIO_000300: 1.668375e6

QD
type: SiteQuality
SIO_000300: 1.428e1

VQSLOD
type: SiteQuality
SIO_000300: 6.820000000000001e-1

FS
type: SiteQuality
SIO_000300: 2.124e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.63e-1

GenotypeQuality
all individuals: 132
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8813
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28522
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5430
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3260
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2100
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 979
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2784
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13636
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10204
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.540404818386272e-5
allele num: 64918
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

QD
type: SiteQuality
SIO_000300: 1.454e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.122e0

FS
type: SiteQuality
SIO_000300: 3.746e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.81e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.947e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.77e0

MQRankSum
type: SiteQuality
SIO_000300: -1.698e0

DP
type: SiteQuality
SIO_000300: 1.650361e6

GenotypeQuality
all individuals: 1043
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5654
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1130
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2781
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4197
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 8788
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28144
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2098
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 838
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.07918105574741e-4
allele num: 64864
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10200
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13602
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.498e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

QD
type: SiteQuality
SIO_000300: 1.355e1

DP
type: SiteQuality
SIO_000300: 1.644815e6

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.944e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.09e-1

GenotypeQuality
all individuals: 401
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1092
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1761
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3215
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4197
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 2084
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12756
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.554678026180778e-5
allele num: 64322
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 6.110335195530726e-4
allele num: 11456
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8476
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.899029895070283e-5
allele num: 10102
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.024e0

QD
type: SiteQuality
SIO_000300: 1.561e1

MQRankSum
type: SiteQuality
SIO_000300: -5.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e0

DP
type: SiteQuality
SIO_000300: 1.590564e6

MQ
type: SiteQuality
SIO_000300: 5.89e1

VQSLOD
type: SiteQuality
SIO_000300: 2.69e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e-1

GenotypeQuality
all individuals: 770
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3503
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18836
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4187
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63690
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11414
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9944
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.378016085790885e-5
allele num: 11936
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8392
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.557844e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

FS
type: SiteQuality
SIO_000300: 4.184e0

VQSLOD
type: SiteQuality
SIO_000300: -2.535e0

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.600000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.531e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.9e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 7

GenotypeQuality
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GenotypeQuality
all individuals: 2026
bin: 8.25e1
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GenotypeQuality
all individuals: 791
bin: 5.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11958
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.418856550814731e-5
allele num: 63702
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8386
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.005429318318922e-4
allele num: 9946
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.554822e6

FS
type: SiteQuality
SIO_000300: 1.0615e1

MQRankSum
type: SiteQuality
SIO_000300: -2.407e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.62e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.557e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

MQ
type: SiteQuality
SIO_000300: 5.483e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.4e-2

QD
type: SiteQuality
SIO_000300: 3.67e0

GenotypeQuality
all individuals: 487
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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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bin: 9.75e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6725
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2368
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11392
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8388
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12006
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.004823151125402e-4
allele num: 9952
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63658
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.682e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.49e0

FS
type: SiteQuality
SIO_000300: 2.674e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.391e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.098e0

DP
type: SiteQuality
SIO_000300: 1.552991e6

QD
type: SiteQuality
SIO_000300: 5.64e0

GenotypeQuality
all individuals: 2021
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1517
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GenotypeQuality
all individuals: 136
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6668
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 1.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11830
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63468
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.009896990506968e-4
allele num: 9902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11376
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8362
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

DP
type: SiteQuality
SIO_000300: 1.54361e6

FS
type: SiteQuality
SIO_000300: 2.925e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.390000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

VQSLOD
type: SiteQuality
SIO_000300: -1.354e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

GenotypeQuality
all individuals: 7218
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66346
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.723842862699339e-5
allele num: 10284
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
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: 902
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.222000995520159e-5
allele num: 16072
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.673077e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.427e1

MQRankSum
type: SiteQuality
SIO_000300: 6.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.99e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.8e-2

FS
type: SiteQuality
SIO_000300: 8.582000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.53e-1

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1515
bin: 9.75e1
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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1589
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10280
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.195019204559534e-5
allele num: 16142
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: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66356
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

MQRankSum
type: SiteQuality
SIO_000300: 8.97e-1

DP
type: SiteQuality
SIO_000300: 1.673627e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.14e0

VQSLOD
type: SiteQuality
SIO_000300: -3.222e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

FS
type: SiteQuality
SIO_000300: 1.992e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.13e-2

QD
type: SiteQuality
SIO_000300: 1.652e1

GenotypeQuality
all individuals: 44122
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1514
bin: 9.75e1
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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 700
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 317
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variant carriers: 0

GenotypeQuality
all individuals: 548
bin: 3.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 3
allele frequency: 2.914319020788809e-4
allele num: 10294
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16156
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: 0
allele frequency: 0.0e0
allele num: 66376
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.67645e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.27e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.17e-1

QD
type: SiteQuality
SIO_000300: 1.772e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.51e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 402
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1510
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variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7262
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1587
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.164468006411046e-5
allele num: 16222
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66426
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: 904
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.689547e6

MQRankSum
type: SiteQuality
SIO_000300: 6.23e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.21e-1

QD
type: SiteQuality
SIO_000300: 1.441e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.281e0

MQ
type: SiteQuality
SIO_000300: 5.875e1

VQSLOD
type: SiteQuality
SIO_000300: -7.95e-2

GenotypeQuality
all individuals: 235
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7302
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1509
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 219
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 379
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1578
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variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 702
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variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1486
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.708737864077671e-5
allele num: 10300
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66464
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16256
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.95e1

VQSLOD
type: SiteQuality
SIO_000300: 2.76e0

QD
type: SiteQuality
SIO_000300: 1.208e1

FS
type: SiteQuality
SIO_000300: 8.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.49e-1

DP
type: SiteQuality
SIO_000300: 1.693639e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.91e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.27e-2

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7293
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1597
bin: 9.75e1
variant carriers: 4

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

GenotypeQuality
all individuals: 282
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.75e1
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GenotypeQuality
all individuals: 180
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 2.75e1
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GenotypeQuality
all individuals: 80
bin: 4.75e1
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GenotypeQuality
all individuals: 236
bin: 8.75e1
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GenotypeQuality
all individuals: 46301
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 9.25e1
variant carriers: 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: 8630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10314
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: 4
allele frequency: 2.455494168201351e-4
allele num: 16290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66478
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 3.59e0

MQRankSum
type: SiteQuality
SIO_000300: 2.73e-1

FS
type: SiteQuality
SIO_000300: 1.459e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.370000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.73e0

QD
type: SiteQuality
SIO_000300: 1.66e1

DP
type: SiteQuality
SIO_000300: 1.714885e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.75e-1

GenotypeQuality
all individuals: 282
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1484
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1576
bin: 7.25e1
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GenotypeQuality
all individuals: 180
bin: 3.75e1
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GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 346
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 172
bin: 2.75e1
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GenotypeQuality
all individuals: 80
bin: 4.75e1
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GenotypeQuality
all individuals: 236
bin: 8.75e1
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GenotypeQuality
all individuals: 699
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variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46301
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.805108456933121e-4
allele num: 66478
num of homozygotes: 0

Latino
type: Population
allele count: 29
allele frequency: 2.510387811634349e-3
allele num: 11552
num of homozygotes: 0

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

African
type: Population
allele count: 643
allele frequency: 6.234244715920109e-2
allele num: 10314
num of homozygotes: 23

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16290
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 5.530973451327434e-3
allele num: 904
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.714885e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.370000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.66e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.73e0

MQRankSum
type: SiteQuality
SIO_000300: 2.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.59e0

FS
type: SiteQuality
SIO_000300: 1.459e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-2

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

GenotypeQuality
all individuals: 3
bin: 1.25e1
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GenotypeQuality
all individuals: 109
bin: 2.75e1
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GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 250
bin: 9.25e1
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GenotypeQuality
all individuals: 83
bin: 3.75e1
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GenotypeQuality
all individuals: 140
bin: 3.25e1
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GenotypeQuality
all individuals: 269
bin: 2.25e1
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GenotypeQuality
all individuals: 47
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GenotypeQuality
all individuals: 951
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GenotypeQuality
all individuals: 1598
bin: 7.25e1
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GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 7401
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47235
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 3
allele frequency: 2.901915264074289e-4
allele num: 10338
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: 8630
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: 66514
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16340
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
type: SiteQuality
SIO_000300: 5.25e-1

FS
type: SiteQuality
SIO_000300: 3.995e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.624e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.81e-1

QD
type: SiteQuality
SIO_000300: 1.189e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.24e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

DP
type: SiteQuality
SIO_000300: 1.671293e6

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

GenotypeQuality
all individuals: 56
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 5

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1504
bin: 7.75e1
variant carriers: 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: 10368
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: 5
allele frequency: 3.038405444822557e-4
allele num: 16456
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66564
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.477e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

VQSLOD
type: SiteQuality
SIO_000300: 8.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.91e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.55e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.933e1

DP
type: SiteQuality
SIO_000300: 1.676863e6

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 298

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1500
bin: 7.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999220202747286e-5
allele num: 66684
num of homozygotes: 0

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

African
type: Population
allele count: 287
allele frequency: 2.759615384615385e-2
allele num: 10400
num of homozygotes: 4

Latino
type: Population
allele count: 13
allele frequency: 1.123013130615066e-3
allele num: 11576
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.701675e6

MQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.82e0

VQSLOD
type: SiteQuality
SIO_000300: 5.63e0

QD
type: SiteQuality
SIO_000300: 1.422e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.39e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.26e-2

GenotypeQuality
all individuals: 700
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1508
bin: 7.75e1
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7536
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

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

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.668986e6

MQ
type: SiteQuality
SIO_000300: 5.983e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

FS
type: SiteQuality
SIO_000300: 3.566e0

VQSLOD
type: SiteQuality
SIO_000300: 7.97e-1

QD
type: SiteQuality
SIO_000300: 1.124e1

MQRankSum
type: SiteQuality
SIO_000300: -3.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.957e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.85e-1

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 9
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
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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
all individuals: 2
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1617
bin: 7.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 2.969e0

MQRankSum
type: SiteQuality
SIO_000300: 1.75e-1

DP
type: SiteQuality
SIO_000300: 1.669107e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.46e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 9.87e-1

QD
type: SiteQuality
SIO_000300: 1.354e1

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

GenotypeQuality
all individuals: 696
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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GenotypeQuality
all individuals: 2
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variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
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: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.179e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

FS
type: SiteQuality
SIO_000300: 1.098e0

VQSLOD
type: SiteQuality
SIO_000300: 8.62e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.9e0

MQRankSum
type: SiteQuality
SIO_000300: -1.7e-2

DP
type: SiteQuality
SIO_000300: 1.669122e6

GenotypeQuality
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bin: 8.25e1
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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 692
bin: 9.75e1
variant carriers: 1

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

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

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.432e1

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

MQ
type: SiteQuality
SIO_000300: 5.919e1

FS
type: SiteQuality
SIO_000300: 1.57e0

DP
type: SiteQuality
SIO_000300: 1.668852e6

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.99e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.49243264303054e-5
allele num: 66734
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
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East Asian
type: Population
allele count: 0
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allele num: 8654
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

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

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.031e0

DP
type: SiteQuality
SIO_000300: 1.669156e6

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 8.62e-1

QD
type: SiteQuality
SIO_000300: 1.31e1

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4
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variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.25e1
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: 6614
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996973057212216e-5
allele num: 66734
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

FS
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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QD
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MQ
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

African
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East Asian
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European (Finnish)
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European (Non-Finnish)
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South Asian
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Other
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MQRankSum
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ReadPosRankSum
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FS
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MQ
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DP
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997332374186974e-5
allele num: 66726
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ClippingRankSum
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SIO_000300: 5.88e-1

FS
type: SiteQuality
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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DP
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QD
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VQSLOD
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InbreedingCoeff
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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European (Finnish)
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South Asian
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Latino
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Other
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ReadPosRankSum
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DP
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FS
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MQRankSum
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MQ
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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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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GenotypeQuality
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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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Other
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East Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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MQRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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FS
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MQ
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QD
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
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Other
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Latino
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African
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East Asian
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European (Finnish)
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South Asian
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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VQSLOD
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DP
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ReadPosRankSum
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MQ
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ClippingRankSum
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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African
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Latino
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East Asian
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South Asian
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European (Finnish)
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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QD
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DP
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VQSLOD
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MQRankSum
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MQ
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 9.609840476648087e-5
allele num: 10406
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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Other
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MQ
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BaseQRankSum
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MQRankSum
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VQSLOD
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FS
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InbreedingCoeff
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QD
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ReadPosRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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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African
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

BaseQRankSum
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VQSLOD
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MQ
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DP
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ReadPosRankSum
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InbreedingCoeff
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FS
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QD
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MQRankSum
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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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GenotypeQuality
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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
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num of homozygotes: 0

European (Non-Finnish)
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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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South Asian
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East Asian
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allele num: 8652
num of homozygotes: 0

European (Finnish)
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Other
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DP
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ReadPosRankSum
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InbreedingCoeff
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QD
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FS
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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MQ
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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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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Latino
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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: 1.499160470136723e-5
allele num: 66704
num of homozygotes: 0

East Asian
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ClippingRankSum
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DP
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VQSLOD
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FS
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InbreedingCoeff
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MQ
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MQRankSum
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BaseQRankSum
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QD
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ReadPosRankSum
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SIO_000300: -1.7e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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South Asian
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Latino
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East Asian
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European (Finnish)
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European (Non-Finnish)
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQRankSum
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QD
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ReadPosRankSum
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ClippingRankSum
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FS
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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European (Non-Finnish)
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South Asian
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African
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European (Finnish)
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Latino
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BaseQRankSum
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FS
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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MQRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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European (Non-Finnish)
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Other
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African
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South Asian
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European (Finnish)
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DP
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FS
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MQ
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ClippingRankSum
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MQRankSum
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QD
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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Latino
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African
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East Asian
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European (Finnish)
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European (Non-Finnish)
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VQSLOD
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FS
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QD
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ReadPosRankSum
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MQ
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InbreedingCoeff
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DP
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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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: 904
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 6
allele frequency: 9.006304413089163e-5
allele num: 66620
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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InbreedingCoeff
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SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 1.287e0

QD
type: SiteQuality
SIO_000300: 1.29e1

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

DP
type: SiteQuality
SIO_000300: 1.660479e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.49e0

MQRankSum
type: SiteQuality
SIO_000300: 9.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.18e-1

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

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

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

African
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allele count: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
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: 11518
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
type: SiteQuality
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VQSLOD
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BaseQRankSum
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SIO_000300: -3.84e0

QD
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SIO_000300: 1.162e1

ClippingRankSum
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SIO_000300: -3.4e-2

FS
type: SiteQuality
SIO_000300: 5.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 1.659422e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.71e-1

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

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

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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 7.04e-1

FS
type: SiteQuality
SIO_000300: 5.92e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

BaseQRankSum
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SIO_000300: -3.84e0

DP
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SIO_000300: 1.659422e6

QD
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SIO_000300: 1.162e1

ReadPosRankSum
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SIO_000300: -1.71e-1

ClippingRankSum
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SIO_000300: -3.4e-2

VQSLOD
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SIO_000300: 1.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11342
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.57e-1

DP
type: SiteQuality
SIO_000300: 1.612864e6

FS
type: SiteQuality
SIO_000300: 4.639e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.55e-1

QD
type: SiteQuality
SIO_000300: 1.399e1

MQ
type: SiteQuality
SIO_000300: 5.954e1

VQSLOD
type: SiteQuality
SIO_000300: 9.68e-1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6464
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11342
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.048501661433405e-5
allele num: 65606
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.612864e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

FS
type: SiteQuality
SIO_000300: 4.639e0

VQSLOD
type: SiteQuality
SIO_000300: 9.68e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 3.55e-1

BaseQRankSum
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SIO_000300: 2.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.57e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 2
allele frequency: 1.231527093596059e-4
allele num: 16240
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.552553951249806e-5
allele num: 64410
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11088
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.565958e6

QD
type: SiteQuality
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 5.96e1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.885e0

BaseQRankSum
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SIO_000300: -4.278e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10136
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.559089491736826e-5
allele num: 64140
num of homozygotes: 0

European (Finnish)
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ClippingRankSum
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SIO_000300: 1.06e0

DP
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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QD
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.961e1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.577038322031225e-5
allele num: 63410
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
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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South Asian
type: Population
allele count: 0
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.14e0

InbreedingCoeff
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DP
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FS
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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VQSLOD
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QD
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3518
bin: 6.75e1
variant carriers: 1

Latino
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allele count: 5
allele frequency: 6.208095356344674e-4
allele num: 8054
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8686
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5104
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6310
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 7.718431614695894e-5
allele num: 51824
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14348
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.154463e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.854e0

QD
type: SiteQuality
SIO_000300: 1.391e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.93e0

FS
type: SiteQuality
SIO_000300: 1.129e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.98e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.95e-1

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.051780752715332e-5
allele num: 39590
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6968
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4012
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5740
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12678
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.711e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-1

ReadPosRankSum
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.883e1

FS
type: SiteQuality
SIO_000300: 2.062e0

DP
type: SiteQuality
SIO_000300: 8.40679e5

MQRankSum
type: SiteQuality
SIO_000300: -5.4e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.531e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.23e-2

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3096
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3990
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5722
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.823010411152286e-5
allele num: 11334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3336
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30762
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 462
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.33e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.81e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.177e1

DP
type: SiteQuality
SIO_000300: 7.0232e5

MQRankSum
type: SiteQuality
SIO_000300: 5.39e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.43e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 248
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2680
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 7.763975155279503e-4
allele num: 2576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26060
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3082
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5004
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 432
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10604
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.06e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.007e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.635e0

VQSLOD
type: SiteQuality
SIO_000300: 1.23e-1

DP
type: SiteQuality
SIO_000300: 6.45697e5

GenotypeQuality
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bin: 2.75e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 304
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1462
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3278
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1408
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8862
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.1e0

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.92e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.017e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.26e0

MQ
type: SiteQuality
SIO_000300: 5.456e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e0

DP
type: SiteQuality
SIO_000300: 4.98891e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1372
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15774
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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1402
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1312
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FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
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DP
type: SiteQuality
SIO_000300: 4.86237e5

MQRankSum
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
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SIO_000300: 9.88e-1

MQ
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 590
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.824858757062147e-3
allele num: 708
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 454
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
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.09e0

QD
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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MQ
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MQRankSum
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ReadPosRankSum
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 1884
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.185677021579322e-4
allele num: 8434
num of homozygotes: 0

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

MQ
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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QD
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InbreedingCoeff
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SIO_000300: -6.900000000000001e-2

FS
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VQSLOD
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DP
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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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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1449
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 486
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 234
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1718
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.300728407908429e-4
allele num: 7688
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6206
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 606
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

VQSLOD
type: SiteQuality
SIO_000300: 4.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.291e0

DP
type: SiteQuality
SIO_000300: 3.12361e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.28e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.057e0

QD
type: SiteQuality
SIO_000300: 1.888e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 1099
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7358
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 476
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5944
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 586
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 210
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1632
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 164
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 7.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.51e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.08811e5

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 6.345177664974619e-4
allele num: 1576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.380071763731714e-4
allele num: 7246
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 160
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5782
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.67e-2

QD
type: SiteQuality
SIO_000300: 1.178e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.08904e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

VQSLOD
type: SiteQuality
SIO_000300: -1.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.89e-1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 7

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1287
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 7
allele frequency: 6.841282251759187e-4
allele num: 10232
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65894
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15090
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

QD
type: SiteQuality
SIO_000300: 1.272e1

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.336e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.8e-2

FS
type: SiteQuality
SIO_000300: 8.247999999999999e0

DP
type: SiteQuality
SIO_000300: 3.239e6

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 811
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variant carriers: 0

GenotypeQuality
all individuals: 509
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.55276656448235e-5
allele num: 65894
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15090
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.23e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

FS
type: SiteQuality
SIO_000300: 8.247999999999999e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.336e0

DP
type: SiteQuality
SIO_000300: 3.239e6

QD
type: SiteQuality
SIO_000300: 1.272e1

GenotypeQuality
all individuals: 917
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
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variant carriers: 0

GenotypeQuality
all individuals: 72
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10238
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.031956824934813e-5
allele num: 65964
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15210
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.94e-1

FS
type: SiteQuality
SIO_000300: 7.95e0

DP
type: SiteQuality
SIO_000300: 3.239683e6

MQRankSum
type: SiteQuality
SIO_000300: 5.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.03e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

QD
type: SiteQuality
SIO_000300: 1.553e1

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
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GenotypeQuality
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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: 73
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65978
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.832944470368642e-4
allele num: 8572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 3.243032e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.73e-1

QD
type: SiteQuality
SIO_000300: 1.225e1

MQ
type: SiteQuality
SIO_000300: 5.927e1

MQRankSum
type: SiteQuality
SIO_000300: 3.57e-1

FS
type: SiteQuality
SIO_000300: 5.144e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

VQSLOD
type: SiteQuality
SIO_000300: 4.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.699e0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15324
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: 10246
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5148760831364e-5
allele num: 66012
num of homozygotes: 0

Latino
type: Population
allele count: 0
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allele num: 11528
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.247339e6

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.313e1

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.885e1

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 663
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GenotypeQuality
all individuals: 126
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15384
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514279657167086e-5
allele num: 66038
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.728e0

MQRankSum
type: SiteQuality
SIO_000300: 6.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.91e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

VQSLOD
type: SiteQuality
SIO_000300: -4.669e-1

DP
type: SiteQuality
SIO_000300: 3.252432e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 7.61e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e0

GenotypeQuality
all individuals: 971
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46350
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1325
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1725
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1081
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4003
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 981
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10276
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66092
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.471654154801968e-5
allele num: 15452
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
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: 890
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.51e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.92e1

FS
type: SiteQuality
SIO_000300: 8.827999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.92e0

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.43e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.017e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.89e-1

DP
type: SiteQuality
SIO_000300: 3.259535e6

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 971
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 668
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1019
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1725
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1322
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 927
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46350
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 118
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10280
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.671522719389525e-5
allele num: 11532
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66108
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15480
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.222e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.14e-1

QD
type: SiteQuality
SIO_000300: 1.24e1

MQRankSum
type: SiteQuality
SIO_000300: -1.308e0

DP
type: SiteQuality
SIO_000300: 3.263587e6

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

MQ
type: SiteQuality
SIO_000300: 5.803e1

GenotypeQuality
all individuals: 456
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1088
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 971
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 681
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1727
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46355
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 784
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5164
bin: 6.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
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: 2
allele frequency: 3.021148036253776e-5
allele num: 66200
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15724
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.717e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.922e1

MQRankSum
type: SiteQuality
SIO_000300: 1.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.5e-2

DP
type: SiteQuality
SIO_000300: 3.273726e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.87e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.85e-1

QD
type: SiteQuality
SIO_000300: 1.931e1