11-130130937-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130130937
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130130937
    reference: chr 11
allele count: 461
allele frequency: 3.817362790235501e-3
allele num: 120764
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.890A>G
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.832A>G
  hgvsp: ENSP00000350574.4:p.Thr278Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.393A>G
  hgvsp: ENSP00000432558.1:p.Thr132Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.832A>G
  hgvsp: ENSP00000434177.1:p.Thr278Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000435413
  ensembl transcript: ENST00000528448
  gene symbol: ZBTB44
  hgvsc: ENST00000528448.2:c.71A>G
  hgvsp: ENSP00000435413.2:p.Thr25Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.832A>G
  hgvsp: ENSP00000380861.1:p.Thr278Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.832A>G
  hgvsp: ENSP00000433457.1:p.Thr278Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.821A>G
  hgvsp: ENSP00000436187.1:p.Thr275Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.832A>G
  hgvsp: ENSP00000408079.1:p.Thr278Ala
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 20644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5131
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 9.75e1
  variant carriers: 396
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6084
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr278Ala
num of homozygotes: 12
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/11-130130954-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130130954
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130130954
    reference: chr 11
allele count: 1
allele frequency: 8.281024859636628e-6
allele num: 120758
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.815G>T
  hgvsp: ENSP00000350574.4:p.Cys272Phe
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.815G>T
  hgvsp: ENSP00000380861.1:p.Cys272Phe
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.376G>T
  hgvsp: ENSP00000432558.1:p.Cys126Phe
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.873G>T
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.804G>T
  hgvsp: ENSP00000436187.1:p.Cys269Phe
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.815G>T
  hgvsp: ENSP00000408079.1:p.Cys272Phe
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000435413
  ensembl transcript: ENST00000528448
  gene symbol: ZBTB44
  hgvsc: ENST00000528448.2:c.54G>T
  hgvsp: ENSP00000435413.2:p.Cys19Phe
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.815G>T
  hgvsp: ENSP00000434177.1:p.Cys272Phe
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.815G>T
  hgvsp: ENSP00000433457.1:p.Cys272Phe
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20852
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3821
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1503
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Cys272Phe
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

11-130130958-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130130958
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130130958
    reference: chr 11
allele count: 1
allele frequency: 8.281299170213822e-6
allele num: 120754
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.800A>T
  hgvsp: ENSP00000436187.1:p.Thr268Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000435413
  ensembl transcript: ENST00000528448
  gene symbol: ZBTB44
  hgvsc: ENST00000528448.2:c.50A>T
  hgvsp: ENSP00000435413.2:p.Thr18Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.811A>T
  hgvsp: ENSP00000380861.1:p.Thr271Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.811A>T
  hgvsp: ENSP00000433457.1:p.Thr271Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.811A>T
  hgvsp: ENSP00000350574.4:p.Thr271Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.372A>T
  hgvsp: ENSP00000432558.1:p.Thr125Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.811A>T
  hgvsp: ENSP00000434177.1:p.Thr271Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.811A>T
  hgvsp: ENSP00000408079.1:p.Thr271Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.869A>T
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20848
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6148
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 628
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Thr271Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

11-130130959-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130130959
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130130959
    reference: chr 11
allele count: 1
allele frequency: 8.281299170213822e-6
allele num: 120754
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.371G>C
  hgvsp: ENST00000529982.1:c.371G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.868G>C
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000435413
  ensembl transcript: ENST00000528448
  gene symbol: ZBTB44
  hgvsc: ENST00000528448.2:c.49G>C
  hgvsp: ENST00000528448.2:c.49G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.810G>C
  hgvsp: ENST00000530205.1:c.810G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.810G>C
  hgvsp: ENST00000397753.1:c.810G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.810G>C
  hgvsp: ENST00000525842.1:c.810G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.799G>C
  hgvsp: ENST00000527478.1:c.799G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.810G>C
  hgvsp: ENST00000445008.2:c.810G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.810G>C
  hgvsp: ENST00000357899.4:c.810G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6149
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val270Val
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

11-130130963-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130130963
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130130963
    reference: chr 11
allele count: 1
allele frequency: 8.281573498964803e-6
allele num: 120750
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.806A>T
  hgvsp: ENSP00000433457.1:p.Tyr269Phe
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.806A>T
  hgvsp: ENSP00000434177.1:p.Tyr269Phe
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.367A>T
  hgvsp: ENSP00000432558.1:p.Tyr123Phe
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.806A>T
  hgvsp: ENSP00000350574.4:p.Tyr269Phe
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.806A>T
  hgvsp: ENSP00000408079.1:p.Tyr269Phe
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000435413
  ensembl transcript: ENST00000528448
  gene symbol: ZBTB44
  hgvsc: ENST00000528448.2:c.45A>T
  hgvsp: ENSP00000435413.2:p.Tyr16Phe
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.864A>T
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.806A>T
  hgvsp: ENSP00000380861.1:p.Tyr269Phe
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.795A>T
  hgvsp: ENSP00000436187.1:p.Tyr266Phe
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20843
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28096
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Tyr269Phe
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

11-130130966-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130130966
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130130966
    reference: chr 11
allele count: 1
allele frequency: 8.281847845891375e-6
allele num: 120746
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.364A>G
  hgvsp: ENSP00000432558.1:p.Asp122Gly
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000435413
  ensembl transcript: ENST00000528448
  gene symbol: ZBTB44
  hgvsc: ENST00000528448.2:c.42A>G
  hgvsp: ENSP00000435413.2:p.Asp15Gly
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.792A>G
  hgvsp: ENSP00000436187.1:p.Asp265Gly
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.803A>G
  hgvsp: ENSP00000350574.4:p.Asp268Gly
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.803A>G
  hgvsp: ENSP00000433457.1:p.Asp268Gly
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.803A>G
  hgvsp: ENSP00000380861.1:p.Asp268Gly
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.861A>G
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.803A>G
  hgvsp: ENSP00000408079.1:p.Asp268Gly
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.803A>G
  hgvsp: ENSP00000434177.1:p.Asp268Gly
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45227
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp268Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/11-130130967-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130130967
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130130967
    reference: chr 11
allele count: 1
allele frequency: 8.282122210995345e-6
allele num: 120742
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.363G>T
  hgvsp: ENSP00000432558.1:p.Asp122Tyr
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.802G>T
  hgvsp: ENSP00000380861.1:p.Asp268Tyr
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.802G>T
  hgvsp: ENSP00000350574.4:p.Asp268Tyr
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.802G>T
  hgvsp: ENSP00000408079.1:p.Asp268Tyr
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000435413
  ensembl transcript: ENST00000528448
  gene symbol: ZBTB44
  hgvsc: ENST00000528448.2:c.41G>T
  hgvsp: ENSP00000435413.2:p.Asp15Tyr
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.791G>T
  hgvsp: ENSP00000436187.1:p.Asp265Tyr
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.860G>T
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.802G>T
  hgvsp: ENSP00000433457.1:p.Asp268Tyr
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.802G>T
  hgvsp: ENSP00000434177.1:p.Asp268Tyr
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6146
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp268Tyr
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP

11-130130969-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130130969
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130130969
    reference: chr 11
allele count: 1
allele frequency: 8.282670995742708e-6
allele num: 120734
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.800C>T
  hgvsp: ENSP00000434177.1:p.Ala267Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.789C>T
  hgvsp: ENSP00000436187.1:p.Ala264Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000435413
  ensembl transcript: ENST00000528448
  gene symbol: ZBTB44
  hgvsc: ENST00000528448.2:c.39C>T
  hgvsp: ENSP00000435413.2:p.Ala14Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.800C>T
  hgvsp: ENSP00000433457.1:p.Ala267Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.800C>T
  hgvsp: ENSP00000350574.4:p.Ala267Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.858C>T
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.800C>T
  hgvsp: ENSP00000408079.1:p.Ala267Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.361C>T
  hgvsp: ENSP00000432558.1:p.Ala121Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.800C>T
  hgvsp: ENSP00000380861.1:p.Ala267Val
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala267Val
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

11-130130974-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130130974
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130130974
    reference: chr 11
allele count: 8
allele frequency: 6.62712482189602e-5
allele num: 120716
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.784A>G
  hgvsp: ENST00000527478.1:c.784A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.795A>G
  hgvsp: ENST00000445008.2:c.795A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.795A>G
  hgvsp: ENST00000357899.4:c.795A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.853A>G
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.795A>G
  hgvsp: ENST00000525842.1:c.795A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.356A>G
  hgvsp: ENST00000529982.1:c.356A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.795A>G
  hgvsp: ENST00000397753.1:c.795A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.795A>G
  hgvsp: ENST00000530205.1:c.795A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000435413
  ensembl transcript: ENST00000528448
  gene symbol: ZBTB44
  hgvsc: ENST00000528448.2:c.34A>G
  hgvsp: ENST00000528448.2:c.34A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6137
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1498
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg265Arg
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS

11-130130976-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130130976
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130130976
    reference: chr 11
allele count: 1
allele frequency: 8.283906027370025e-6
allele num: 120716
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.793A>C
  hgvsp: ENST00000445008.2:c.793A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.793A>C
  hgvsp: ENST00000397753.1:c.793A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.354A>C
  hgvsp: ENST00000529982.1:c.354A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.793A>C
  hgvsp: ENST00000525842.1:c.793A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.851A>C
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.782A>C
  hgvsp: ENST00000527478.1:c.782A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000435413
  ensembl transcript: ENST00000528448
  gene symbol: ZBTB44
  hgvsc: ENST00000528448.2:c.32A>C
  hgvsp: ENST00000528448.2:c.32A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.793A>C
  hgvsp: ENST00000357899.4:c.793A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.793A>C
  hgvsp: ENST00000530205.1:c.793A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20808
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5194
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 982
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg265Arg
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum

11-130130983-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130130983
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130130983
    reference: chr 11
allele count: 2
allele frequency: 1.657055743355207e-5
allele num: 120696
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.786C>G
  hgvsp: ENST00000445008.2:c.786C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000435413
  ensembl transcript: ENST00000528448
  gene symbol: ZBTB44
  hgvsc: ENST00000528448.2:c.25C>G
  hgvsp: ENST00000528448.2:c.25C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.844C>G
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.786C>G
  hgvsp: ENST00000397753.1:c.786C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.347C>G
  hgvsp: ENST00000529982.1:c.347C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.775C>G
  hgvsp: ENST00000527478.1:c.775C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.786C>G
  hgvsp: ENST00000530205.1:c.786C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.786C>G
  hgvsp: ENST00000357899.4:c.786C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.786C>G
  hgvsp: ENST00000525842.1:c.786C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5169
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28007
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr262Thr
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP

11-130130983-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130130983
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130130983
    reference: chr 11
allele count: 3
allele frequency: 2.48558361503281e-5
allele num: 120696
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.844C>T
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000435413
  ensembl transcript: ENST00000528448
  gene symbol: ZBTB44
  hgvsc: ENST00000528448.2:c.25C>T
  hgvsp: ENST00000528448.2:c.25C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.786C>T
  hgvsp: ENST00000445008.2:c.786C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.786C>T
  hgvsp: ENST00000397753.1:c.786C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.786C>T
  hgvsp: ENST00000525842.1:c.786C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.347C>T
  hgvsp: ENST00000529982.1:c.347C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.786C>T
  hgvsp: ENST00000357899.4:c.786C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.775C>T
  hgvsp: ENST00000527478.1:c.775C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.786C>T
  hgvsp: ENST00000530205.1:c.786C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28007
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5169
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 980
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr262Thr
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

11-130130994-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130130994
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130130994
    reference: chr 11
allele count: 1
allele frequency: 8.286377195889957e-6
allele num: 120680
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.336C>T
  hgvsp: ENSP00000432558.1:p.Pro113Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.775C>T
  hgvsp: ENSP00000350574.4:p.Pro259Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.833C>T
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.775C>T
  hgvsp: ENSP00000408079.1:p.Pro259Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.764C>T
  hgvsp: ENSP00000436187.1:p.Pro256Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.775C>T
  hgvsp: ENSP00000380861.1:p.Pro259Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.775C>T
  hgvsp: ENSP00000433457.1:p.Pro259Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000435413
  ensembl transcript: ENST00000528448
  gene symbol: ZBTB44
  hgvsc: ENST00000528448.2:c.14C>T
  hgvsp: ENSP00000435413.2:p.Pro6Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.775C>T
  hgvsp: ENSP00000434177.1:p.Pro259Ser
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20776
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5160
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27987
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro259Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/11-130130996-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130130996
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130130996
    reference: chr 11
allele count: 1
allele frequency: 8.288162845823595e-6
allele num: 120654
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.773G>T
  hgvsp: ENSP00000380861.1:p.Gly258Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.334G>T
  hgvsp: ENSP00000432558.1:p.Gly112Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.773G>T
  hgvsp: ENSP00000434177.1:p.Gly258Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.831G>T
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.762G>T
  hgvsp: ENSP00000436187.1:p.Gly255Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.773G>T
  hgvsp: ENSP00000408079.1:p.Gly258Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.773G>T
  hgvsp: ENSP00000350574.4:p.Gly258Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000435413
  ensembl transcript: ENST00000528448
  gene symbol: ZBTB44
  hgvsc: ENST00000528448.2:c.12G>T
  hgvsp: ENSP00000435413.2:p.Gly5Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.773G>T
  hgvsp: ENSP00000433457.1:p.Gly258Val
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly258Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

11-130131004-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131004
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131004
    reference: chr 11
allele count: 1
allele frequency: 8.288849839196314e-6
allele num: 120644
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.754A>G
  hgvsp: ENST00000527478.1:c.754A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.765A>G
  hgvsp: ENST00000525842.1:c.765A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.765A>G
  hgvsp: ENST00000530205.1:c.765A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.326A>G
  hgvsp: ENST00000529982.1:c.326A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.765A>G
  hgvsp: ENST00000445008.2:c.765A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.765A>G
  hgvsp: ENST00000357899.4:c.765A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.765A>G
  hgvsp: ENST00000397753.1:c.765A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000435413
  ensembl transcript: ENST00000528448
  gene symbol: ZBTB44
  hgvsc: ENST00000528448.2:c.4A>G
  hgvsp: ENST00000528448.2:c.4A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.823A>G
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6109
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Glu255Glu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS

11-130131012-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131012
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131012
    reference: chr 11
allele count: 3
allele frequency: 2.487479685582568e-5
allele num: 120604
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.757A>G
  hgvsp: ENSP00000433457.1:p.Thr253Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.318A>G
  hgvsp: ENSP00000432558.1:p.Thr107Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.757A>G
  hgvsp: ENSP00000434177.1:p.Thr253Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.757A>G
  hgvsp: ENSP00000350574.4:p.Thr253Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.757A>G
  hgvsp: ENSP00000380861.1:p.Thr253Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.757A>G
  hgvsp: ENSP00000408079.1:p.Thr253Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.746A>G
  hgvsp: ENSP00000436187.1:p.Thr250Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.815A>G
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20735
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27914
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5140
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44856
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr253Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

11-130131014-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131014
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131014
    reference: chr 11
allele count: 2
allele frequency: 1.658402295228776e-5
allele num: 120598
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.755G>A
  hgvsp: ENSP00000350574.4:p.Arg252Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.755G>A
  hgvsp: ENSP00000434177.1:p.Arg252Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.316G>A
  hgvsp: ENSP00000432558.1:p.Arg106Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.755G>A
  hgvsp: ENSP00000380861.1:p.Arg252Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.813G>A
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.755G>A
  hgvsp: ENSP00000433457.1:p.Arg252Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.755G>A
  hgvsp: ENSP00000408079.1:p.Arg252Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.744G>A
  hgvsp: ENSP00000436187.1:p.Arg249Gln
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27905
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20734
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44835
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg252Gln
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

11-130131015-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131015
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131015
    reference: chr 11
allele count: 1
allele frequency: 8.29242404139578e-6
allele num: 120592
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.743C>T
  hgvsp: ENSP00000436187.1:p.Arg249Trp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.754C>T
  hgvsp: ENSP00000408079.1:p.Arg252Trp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.754C>T
  hgvsp: ENSP00000433457.1:p.Arg252Trp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.754C>T
  hgvsp: ENSP00000350574.4:p.Arg252Trp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.754C>T
  hgvsp: ENSP00000380861.1:p.Arg252Trp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.315C>T
  hgvsp: ENSP00000432558.1:p.Arg106Trp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.812C>T
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.754C>T
  hgvsp: ENSP00000434177.1:p.Arg252Trp
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27912
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20730
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1536
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 976
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1496
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg252Trp
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD

11-130131017-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131017
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131017
    reference: chr 11
allele count: 1
allele frequency: 8.291873963515755e-6
allele num: 120600
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.752C>T
  hgvsp: ENSP00000408079.1:p.Thr251Ile
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.810C>T
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.752C>T
  hgvsp: ENSP00000350574.4:p.Thr251Ile
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.741C>T
  hgvsp: ENSP00000436187.1:p.Thr248Ile
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.752C>T
  hgvsp: ENSP00000380861.1:p.Thr251Ile
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.313C>T
  hgvsp: ENSP00000432558.1:p.Thr105Ile
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.752C>T
  hgvsp: ENSP00000434177.1:p.Thr251Ile
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.752C>T
  hgvsp: ENSP00000433457.1:p.Thr251Ile
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20729
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27910
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1536
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr251Ile
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-130131021-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131021
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131021
    reference: chr 11
allele count: 7
allele frequency: 5.804600560558568e-5
allele num: 120594
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.748A>G
  hgvsp: ENSP00000434177.1:p.Asn250Asp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.748A>G
  hgvsp: ENSP00000350574.4:p.Asn250Asp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.737A>G
  hgvsp: ENSP00000436187.1:p.Asn247Asp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.748A>G
  hgvsp: ENSP00000380861.1:p.Asn250Asp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.309A>G
  hgvsp: ENSP00000432558.1:p.Asn104Asp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.748A>G
  hgvsp: ENSP00000433457.1:p.Asn250Asp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.748A>G
  hgvsp: ENSP00000408079.1:p.Asn250Asp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.806A>G
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20724
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3820
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1495
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asn250Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

11-130131025-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131025
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131025
    reference: chr 11
allele count: 1
allele frequency: 8.292974192264313e-6
allele num: 120584
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.744A>G
  hgvsp: ENST00000530205.1:c.744A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.305A>G
  hgvsp: ENST00000529982.1:c.305A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.744A>G
  hgvsp: ENST00000397753.1:c.744A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.744A>G
  hgvsp: ENST00000445008.2:c.744A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.744A>G
  hgvsp: ENST00000525842.1:c.744A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.802A>G
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.733A>G
  hgvsp: ENST00000527478.1:c.733A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.744A>G
  hgvsp: ENST00000357899.4:c.744A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27861
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20734
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5138
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1534
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44793
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6100
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala248Ala
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-130131026-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131026
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131026
    reference: chr 11
allele count: 34
allele frequency: 2.819891848853797e-4
allele num: 120572
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.743C>T
  hgvsp: ENSP00000380861.1:p.Ala248Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.801C>T
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.743C>T
  hgvsp: ENSP00000433457.1:p.Ala248Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.732C>T
  hgvsp: ENSP00000436187.1:p.Ala245Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.743C>T
  hgvsp: ENSP00000408079.1:p.Ala248Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.743C>T
  hgvsp: ENSP00000350574.4:p.Ala248Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.743C>T
  hgvsp: ENSP00000434177.1:p.Ala248Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.304C>T
  hgvsp: ENSP00000432558.1:p.Ala102Val
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20737
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 27835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6090
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala248Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

11-130131026-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131026
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131026
    reference: chr 11
allele count: 4
allele frequency: 3.317519822180938e-5
allele num: 120572
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.732C>G
  hgvsp: ENSP00000436187.1:p.Ala245Gly
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.743C>G
  hgvsp: ENSP00000434177.1:p.Ala248Gly
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.801C>G
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.743C>G
  hgvsp: ENSP00000433457.1:p.Ala248Gly
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.743C>G
  hgvsp: ENSP00000380861.1:p.Ala248Gly
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.304C>G
  hgvsp: ENSP00000432558.1:p.Ala102Gly
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.743C>G
  hgvsp: ENSP00000350574.4:p.Ala248Gly
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.743C>G
  hgvsp: ENSP00000408079.1:p.Ala248Gly
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20737
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 973
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1533
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44796
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala248Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

11-130131028-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131028
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131028
    reference: chr 11
allele count: 1
allele frequency: 8.29324929507381e-6
allele num: 120580
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.741A>G
  hgvsp: ENST00000530205.1:c.741A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.741A>G
  hgvsp: ENST00000445008.2:c.741A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.741A>G
  hgvsp: ENST00000357899.4:c.741A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.741A>G
  hgvsp: ENST00000397753.1:c.741A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.741A>G
  hgvsp: ENST00000525842.1:c.741A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.799A>G
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.730A>G
  hgvsp: ENST00000527478.1:c.730A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.302A>G
  hgvsp: ENST00000529982.1:c.302A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20761
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 971
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln247Gln
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD

11-130131031-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131031
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131031
    reference: chr 11
allele count: 1
allele frequency: 8.29324929507381e-6
allele num: 120580
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.299G>A
  hgvsp: ENST00000529982.1:c.299G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.738G>A
  hgvsp: ENST00000357899.4:c.738G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.738G>A
  hgvsp: ENST00000525842.1:c.738G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.738G>A
  hgvsp: ENST00000397753.1:c.738G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.796G>A
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.738G>A
  hgvsp: ENST00000530205.1:c.738G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.727G>A
  hgvsp: ENST00000527478.1:c.727G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.738G>A
  hgvsp: ENST00000445008.2:c.738G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27791
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20761
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44747
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Lys246Lys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD

11-130131040-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131040
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131040
    reference: chr 11
allele count: 1
allele frequency: 8.294212298657997e-6
allele num: 120566
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.718G>A
  hgvsp: ENST00000527478.1:c.718G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.729G>A
  hgvsp: ENST00000445008.2:c.729G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.729G>A
  hgvsp: ENST00000530205.1:c.729G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.729G>A
  hgvsp: ENST00000357899.4:c.729G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.787G>A
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.290G>A
  hgvsp: ENST00000529982.1:c.290G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.729G>A
  hgvsp: ENST00000397753.1:c.729G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.729G>A
  hgvsp: ENST00000525842.1:c.729G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44676
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu243Glu
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

11-130131055-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131055
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131055
    reference: chr 11
allele count: 2
allele frequency: 1.659035105182826e-5
allele num: 120552
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.275A>C
  hgvsp: ENST00000529982.1:c.275A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.714A>C
  hgvsp: ENST00000397753.1:c.714A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.714A>C
  hgvsp: ENST00000357899.4:c.714A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.703A>C
  hgvsp: ENST00000527478.1:c.703A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.714A>C
  hgvsp: ENST00000525842.1:c.714A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.714A>C
  hgvsp: ENST00000530205.1:c.714A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.772A>C
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.714A>C
  hgvsp: ENST00000445008.2:c.714A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20909
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1540
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44227
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6044
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg238Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

11-130131056-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131056
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131056
    reference: chr 11
allele count: 1
allele frequency: 8.295726041943191e-6
allele num: 120544
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.713G>A
  hgvsp: ENSP00000350574.4:p.Arg238Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.274G>A
  hgvsp: ENSP00000432558.1:p.Arg92Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.713G>A
  hgvsp: ENSP00000433457.1:p.Arg238Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.713G>A
  hgvsp: ENSP00000380861.1:p.Arg238Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.713G>A
  hgvsp: ENSP00000408079.1:p.Arg238Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.702G>A
  hgvsp: ENSP00000436187.1:p.Arg235Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.713G>A
  hgvsp: ENSP00000434177.1:p.Arg238Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.771G>A
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5165
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20915
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44193
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg238Gln
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/11-130131065-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131065
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131065
    reference: chr 11
allele count: 1
allele frequency: 8.294487483618387e-6
allele num: 120562
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.704G>T
  hgvsp: ENSP00000433457.1:p.Gly235Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.704G>T
  hgvsp: ENSP00000434177.1:p.Gly235Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.704G>T
  hgvsp: ENSP00000350574.4:p.Gly235Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.265G>T
  hgvsp: ENSP00000432558.1:p.Gly89Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.762G>T
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.704G>T
  hgvsp: ENSP00000408079.1:p.Gly235Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.704G>T
  hgvsp: ENSP00000380861.1:p.Gly235Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.693G>T
  hgvsp: ENSP00000436187.1:p.Gly232Val
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1475
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1541
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly235Val
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP

11-130131073-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131073
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131073
    reference: chr 11
allele count: 49
allele frequency: 4.063220392390998e-4
allele num: 120594
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.696T>A
  hgvsp: ENSP00000433457.1:p.Phe232Leu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.754T>A
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.685T>A
  hgvsp: ENSP00000436187.1:p.Phe229Leu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.696T>A
  hgvsp: ENSP00000408079.1:p.Phe232Leu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.257T>A
  hgvsp: ENSP00000432558.1:p.Phe86Leu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.696T>A
  hgvsp: ENSP00000434177.1:p.Phe232Leu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.696T>A
  hgvsp: ENSP00000350574.4:p.Phe232Leu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.696T>A
  hgvsp: ENSP00000380861.1:p.Phe232Leu
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 21067
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27373
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44580
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6046
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Phe232Leu
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

11-130131082-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131082
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131082
    reference: chr 11
allele count: 1
allele frequency: 8.289811821271656e-6
allele num: 120630
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.248T>C
  hgvsp: ENST00000529982.1:c.248T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.676T>C
  hgvsp: ENST00000527478.1:c.676T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.687T>C
  hgvsp: ENST00000445008.2:c.687T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.687T>C
  hgvsp: ENST00000530205.1:c.687T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.687T>C
  hgvsp: ENST00000397753.1:c.687T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.687T>C
  hgvsp: ENST00000357899.4:c.687T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.745T>C
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.687T>C
  hgvsp: ENST00000525842.1:c.687T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3793
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Pro229Pro
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/11-130131082-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131082
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131082
    reference: chr 11
allele count: 5
allele frequency: 4.144905910635829e-5
allele num: 120630
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.687T>G
  hgvsp: ENST00000357899.4:c.687T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.248T>G
  hgvsp: ENST00000529982.1:c.248T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.687T>G
  hgvsp: ENST00000530205.1:c.687T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.687T>G
  hgvsp: ENST00000397753.1:c.687T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.676T>G
  hgvsp: ENST00000527478.1:c.676T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.687T>G
  hgvsp: ENST00000525842.1:c.687T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.745T>G
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.687T>G
  hgvsp: ENST00000445008.2:c.687T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1527
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro229Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

11-130131100-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131100
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131100
    reference: chr 11
allele count: 15
allele frequency: 1.243265644426026e-4
allele num: 120650
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.669C>T
  hgvsp: ENST00000397753.1:c.669C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.727C>T
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.669C>T
  hgvsp: ENST00000525842.1:c.669C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.669C>T
  hgvsp: ENST00000445008.2:c.669C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.658C>T
  hgvsp: ENST00000527478.1:c.658C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.669C>T
  hgvsp: ENST00000530205.1:c.669C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.669C>T
  hgvsp: ENST00000357899.4:c.669C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.230C>T
  hgvsp: ENST00000529982.1:c.230C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5164
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27308
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6060
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp223Asp
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

11-130131108-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131108
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131108
    reference: chr 11
allele count: 37
allele frequency: 3.066874440502636e-4
allele num: 120644
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.661C>T
  hgvsp: ENSP00000380861.1:p.Pro221Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.661C>T
  hgvsp: ENSP00000350574.4:p.Pro221Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.222C>T
  hgvsp: ENSP00000432558.1:p.Pro75Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.661C>T
  hgvsp: ENSP00000433457.1:p.Pro221Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.661C>T
  hgvsp: ENSP00000434177.1:p.Pro221Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.661C>T
  hgvsp: ENSP00000408079.1:p.Pro221Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.650C>T
  hgvsp: ENSP00000436187.1:p.Pro218Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.719C>T
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21445
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5165
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro221Ser
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

11-130131111-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131111
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131111
    reference: chr 11
allele count: 2
allele frequency: 1.657660047077545e-5
allele num: 120652
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.658C>G
  hgvsp: ENSP00000433457.1:p.Gln220Glu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.658C>G
  hgvsp: ENSP00000408079.1:p.Gln220Glu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.658C>G
  hgvsp: ENSP00000350574.4:p.Gln220Glu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.658C>G
  hgvsp: ENSP00000380861.1:p.Gln220Glu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.219C>G
  hgvsp: ENSP00000432558.1:p.Gln74Glu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.658C>G
  hgvsp: ENSP00000434177.1:p.Gln220Glu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.716C>G
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.647C>G
  hgvsp: ENSP00000436187.1:p.Gln217Glu
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5174
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21480
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27243
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1472
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gln220Glu
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

11-130131119-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131119
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131119
    reference: chr 11
allele count: 4
allele frequency: 3.315649867374005e-5
allele num: 120640
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.639A>G
  hgvsp: ENSP00000436187.1:p.Asn214Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.211A>G
  hgvsp: ENSP00000432558.1:p.Asn71Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.650A>G
  hgvsp: ENSP00000433457.1:p.Asn217Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.708A>G
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.650A>G
  hgvsp: ENSP00000350574.4:p.Asn217Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.650A>G
  hgvsp: ENSP00000380861.1:p.Asn217Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.650A>G
  hgvsp: ENSP00000408079.1:p.Asn217Ser
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.650A>G
  hgvsp: ENSP00000434177.1:p.Asn217Ser
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27238
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6064
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asn217Ser
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP

11-130131120-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131120
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131120
    reference: chr 11
allele count: 3
allele frequency: 2.486778626966628e-5
allele num: 120638
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.649A>G
  hgvsp: ENSP00000408079.1:p.Asn217Asp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.707A>G
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.638A>G
  hgvsp: ENSP00000436187.1:p.Asn214Asp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.210A>G
  hgvsp: ENSP00000432558.1:p.Asn71Asp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.649A>G
  hgvsp: ENSP00000433457.1:p.Asn217Asp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.649A>G
  hgvsp: ENSP00000350574.4:p.Asn217Asp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.649A>G
  hgvsp: ENSP00000434177.1:p.Asn217Asp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.649A>G
  hgvsp: ENSP00000380861.1:p.Asn217Asp
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27243
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21526
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 970
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asn217Asp
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

11-130131126-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131126
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131126
    reference: chr 11
allele count: 1
allele frequency: 8.289399515899069e-6
allele num: 120636
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.632T>C
  hgvsp: ENSP00000436187.1:p.Ser212Pro
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.204T>C
  hgvsp: ENSP00000432558.1:p.Ser69Pro
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.643T>C
  hgvsp: ENSP00000434177.1:p.Ser215Pro
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.643T>C
  hgvsp: ENSP00000380861.1:p.Ser215Pro
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.643T>C
  hgvsp: ENSP00000433457.1:p.Ser215Pro
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.643T>C
  hgvsp: ENSP00000350574.4:p.Ser215Pro
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.643T>C
  hgvsp: ENSP00000408079.1:p.Ser215Pro
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.701T>C
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5171
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1529
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser215Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

11-130131127-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131127
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131127
    reference: chr 11
allele count: 1
allele frequency: 8.289399515899069e-6
allele num: 120636
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.642C>T
  hgvsp: ENST00000445008.2:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.642C>T
  hgvsp: ENST00000530205.1:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.700C>T
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.642C>T
  hgvsp: ENST00000525842.1:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.642C>T
  hgvsp: ENST00000357899.4:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.203C>T
  hgvsp: ENST00000529982.1:c.203C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.642C>T
  hgvsp: ENST00000397753.1:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.631C>T
  hgvsp: ENST00000527478.1:c.631C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5169
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6067
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Tyr214Tyr
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

11-130131150-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131150
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131150
    reference: chr 11
allele count: 1
allele frequency: 8.288575028181154e-6
allele num: 120648
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.619G>A
  hgvsp: ENSP00000350574.4:p.Val207Ile
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.619G>A
  hgvsp: ENSP00000408079.1:p.Val207Ile
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.677G>A
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.180G>A
  hgvsp: ENSP00000432558.1:p.Val61Ile
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.619G>A
  hgvsp: ENSP00000434177.1:p.Val207Ile
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.619G>A
  hgvsp: ENSP00000380861.1:p.Val207Ile
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.619G>A
  hgvsp: ENSP00000433457.1:p.Val207Ile
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.608G>A
  hgvsp: ENSP00000436187.1:p.Val204Ile
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27089
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21603
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3776
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val207Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

11-130131152-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131152
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131152
    reference: chr 11
allele count: 1
allele frequency: 8.289124668435012e-6
allele num: 120640
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.617A>G
  hgvsp: ENSP00000408079.1:p.Gln206Arg
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.617A>G
  hgvsp: ENSP00000433457.1:p.Gln206Arg
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.617A>G
  hgvsp: ENSP00000380861.1:p.Gln206Arg
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.606A>G
  hgvsp: ENSP00000436187.1:p.Gln203Arg
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.617A>G
  hgvsp: ENSP00000434177.1:p.Gln206Arg
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.178A>G
  hgvsp: ENSP00000432558.1:p.Gln60Arg
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.617A>G
  hgvsp: ENSP00000350574.4:p.Gln206Arg
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.675A>G
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5190
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6060
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45059
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1529
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gln206Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: T
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

11-130131158-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131158
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131158
    reference: chr 11
allele count: 1
allele frequency: 8.289949265510494e-6
allele num: 120628
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.600C>T
  hgvsp: ENSP00000436187.1:p.Ser201Leu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.611C>T
  hgvsp: ENSP00000434177.1:p.Ser204Leu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.611C>T
  hgvsp: ENSP00000433457.1:p.Ser204Leu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.611C>T
  hgvsp: ENSP00000350574.4:p.Ser204Leu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.611C>T
  hgvsp: ENSP00000380861.1:p.Ser204Leu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.172C>T
  hgvsp: ENSP00000432558.1:p.Ser58Leu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.611C>T
  hgvsp: ENSP00000408079.1:p.Ser204Leu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.669C>T
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21609
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5199
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27045
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6060
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1526
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser204Leu
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/11-130131161-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131161
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131161
    reference: chr 11
allele count: 1
allele frequency: 8.290086714307032e-6
allele num: 120626
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.608G>T
  hgvsp: ENSP00000380861.1:p.Ser203Ile
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.597G>T
  hgvsp: ENSP00000436187.1:p.Ser200Ile
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.608G>T
  hgvsp: ENSP00000408079.1:p.Ser203Ile
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.169G>T
  hgvsp: ENSP00000432558.1:p.Ser57Ile
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.666G>T
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.608G>T
  hgvsp: ENSP00000434177.1:p.Ser203Ile
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.608G>T
  hgvsp: ENSP00000350574.4:p.Ser203Ile
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.608G>T
  hgvsp: ENSP00000433457.1:p.Ser203Ile
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27045
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5194
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21619
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1522
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser203Ile
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

11-130131165-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131165
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131165
    reference: chr 11
allele count: 1
allele frequency: 8.290499088045101e-6
allele num: 120620
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.165A>G
  hgvsp: ENSP00000432558.1:p.Thr56Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.604A>G
  hgvsp: ENSP00000433457.1:p.Thr202Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.604A>G
  hgvsp: ENSP00000408079.1:p.Thr202Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.604A>G
  hgvsp: ENSP00000380861.1:p.Thr202Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.604A>G
  hgvsp: ENSP00000350574.4:p.Thr202Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.662A>G
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.604A>G
  hgvsp: ENSP00000434177.1:p.Thr202Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.593A>G
  hgvsp: ENSP00000436187.1:p.Thr199Ala
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27040
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr202Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

11-130131172-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131172
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131172
    reference: chr 11
allele count: 6
allele frequency: 4.973969559306297e-5
allele num: 120628
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.597C>T
  hgvsp: ENST00000357899.4:c.597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.158C>T
  hgvsp: ENST00000529982.1:c.158C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.597C>T
  hgvsp: ENST00000530205.1:c.597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.597C>T
  hgvsp: ENST00000445008.2:c.597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.597C>T
  hgvsp: ENST00000397753.1:c.597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.586C>T
  hgvsp: ENST00000527478.1:c.586C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.655C>T
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.597C>T
  hgvsp: ENST00000525842.1:c.597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5199
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44981
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1468
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6059
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gly199Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ

11-130131181-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131181
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131181
    reference: chr 11
allele count: 1
allele frequency: 8.289811821271656e-6
allele num: 120630
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.588A>G
  hgvsp: ENST00000530205.1:c.588A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.588A>G
  hgvsp: ENST00000397753.1:c.588A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.588A>G
  hgvsp: ENST00000357899.4:c.588A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.588A>G
  hgvsp: ENST00000525842.1:c.588A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.577A>G
  hgvsp: ENST00000527478.1:c.577A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.149A>G
  hgvsp: ENST00000529982.1:c.149A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.588A>G
  hgvsp: ENST00000445008.2:c.588A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.646A>G
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5198
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26927
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Val196Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ

11-130131192-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131192
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131192
    reference: chr 11
allele count: 1
allele frequency: 8.290774026663129e-6
allele num: 120616
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.635G>C
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.577G>C
  hgvsp: ENSP00000434177.1:p.Glu193Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.138G>C
  hgvsp: ENSP00000432558.1:p.Glu47Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.577G>C
  hgvsp: ENSP00000380861.1:p.Glu193Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.566G>C
  hgvsp: ENSP00000436187.1:p.Glu190Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.577G>C
  hgvsp: ENSP00000350574.4:p.Glu193Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.577G>C
  hgvsp: ENSP00000408079.1:p.Glu193Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.577G>C
  hgvsp: ENSP00000433457.1:p.Glu193Gln
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21713
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5204
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26907
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3776
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu193Gln
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

11-130131197-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131197
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131197
    reference: chr 11
allele count: 1
allele frequency: 8.290086714307032e-6
allele num: 120626
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.572C>T
  hgvsp: ENSP00000434177.1:p.Ser191Phe
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.561C>T
  hgvsp: ENSP00000436187.1:p.Ser188Phe
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.630C>T
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.572C>T
  hgvsp: ENSP00000408079.1:p.Ser191Phe
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.572C>T
  hgvsp: ENSP00000380861.1:p.Ser191Phe
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.572C>T
  hgvsp: ENSP00000433457.1:p.Ser191Phe
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.572C>T
  hgvsp: ENSP00000350574.4:p.Ser191Phe
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.133C>T
  hgvsp: ENSP00000432558.1:p.Ser45Phe
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21730
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5200
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26903
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser191Phe
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-130131200-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131200
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131200
    reference: chr 11
allele count: 2
allele frequency: 1.657907389293234e-5
allele num: 120634
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.558T>G
  hgvsp: ENSP00000436187.1:p.Met187Arg
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.569T>G
  hgvsp: ENSP00000350574.4:p.Met190Arg
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.569T>G
  hgvsp: ENSP00000433457.1:p.Met190Arg
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.130T>G
  hgvsp: ENSP00000432558.1:p.Met44Arg
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.569T>G
  hgvsp: ENSP00000380861.1:p.Met190Arg
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.569T>G
  hgvsp: ENSP00000408079.1:p.Met190Arg
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.569T>G
  hgvsp: ENSP00000434177.1:p.Met190Arg
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.627T>G
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26900
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21741
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5198
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3776
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Met190Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

11-130131207-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131207
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131207
    reference: chr 11
allele count: 5
allele frequency: 4.144768473233085e-5
allele num: 120634
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.562A>G
  hgvsp: ENSP00000408079.1:p.Ile188Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.123A>G
  hgvsp: ENSP00000432558.1:p.Ile42Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.562A>G
  hgvsp: ENSP00000433457.1:p.Ile188Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.562A>G
  hgvsp: ENSP00000380861.1:p.Ile188Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.620A>G
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.562A>G
  hgvsp: ENSP00000350574.4:p.Ile188Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.562A>G
  hgvsp: ENSP00000434177.1:p.Ile188Val
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.551A>G
  hgvsp: ENSP00000436187.1:p.Ile185Val
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21757
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6041
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3777
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ile188Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-130131228-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131228
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131228
    reference: chr 11
allele count: 1
allele frequency: 8.28775070445881e-6
allele num: 120660
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.530C>T
  hgvsp: ENSP00000436187.1:p.Arg178Trp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.541C>T
  hgvsp: ENSP00000434177.1:p.Arg181Trp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.102C>T
  hgvsp: ENSP00000432558.1:p.Arg35Trp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.541C>T
  hgvsp: ENSP00000408079.1:p.Arg181Trp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.541C>T
  hgvsp: ENSP00000380861.1:p.Arg181Trp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.541C>T
  hgvsp: ENSP00000433457.1:p.Arg181Trp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.541C>T
  hgvsp: ENSP00000350574.4:p.Arg181Trp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.599C>T
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21856
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26887
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1441
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg181Trp
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

11-130131236-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131236
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131236
    reference: chr 11
allele count: 2
allele frequency: 1.657330372236402e-5
allele num: 120676
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.533G>A
  hgvsp: ENSP00000433457.1:p.Arg178Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.533G>A
  hgvsp: ENSP00000380861.1:p.Arg178Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.533G>A
  hgvsp: ENSP00000350574.4:p.Arg178Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.533G>A
  hgvsp: ENSP00000434177.1:p.Arg178Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.94G>A
  hgvsp: ENSP00000432558.1:p.Arg32Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.522G>A
  hgvsp: ENSP00000436187.1:p.Arg175Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.591G>A
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.533G>A
  hgvsp: ENSP00000408079.1:p.Arg178Gln
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26932
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1484
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6018
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45310
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg178Gln
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-130131237-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131237
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131237
    reference: chr 11
allele count: 1
allele frequency: 8.286102548805144e-6
allele num: 120684
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.532C>G
  hgvsp: ENSP00000350574.4:p.Arg178Gly
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.532C>G
  hgvsp: ENSP00000408079.1:p.Arg178Gly
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.93C>G
  hgvsp: ENSP00000432558.1:p.Arg32Gly
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.521C>G
  hgvsp: ENSP00000436187.1:p.Arg175Gly
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.590C>G
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.532C>G
  hgvsp: ENSP00000380861.1:p.Arg178Gly
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.532C>G
  hgvsp: ENSP00000433457.1:p.Arg178Gly
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.532C>G
  hgvsp: ENSP00000434177.1:p.Arg178Gly
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26927
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3777
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg178Gly
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

11-130131240-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131240
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131240
    reference: chr 11
allele count: 1
allele frequency: 8.285004142502071e-6
allele num: 120700
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.529T>C
  hgvsp: ENSP00000434177.1:p.Cys177Arg
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.518T>C
  hgvsp: ENSP00000436187.1:p.Cys174Arg
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.587T>C
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.529T>C
  hgvsp: ENSP00000380861.1:p.Cys177Arg
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.529T>C
  hgvsp: ENSP00000350574.4:p.Cys177Arg
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.90T>C
  hgvsp: ENSP00000432558.1:p.Cys31Arg
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.529T>C
  hgvsp: ENSP00000433457.1:p.Cys177Arg
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.529T>C
  hgvsp: ENSP00000408079.1:p.Cys177Arg
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21921
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1494
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Cys177Arg
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD

11-130131252-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131252
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131252
    reference: chr 11
allele count: 1
allele frequency: 8.284592315212168e-6
allele num: 120706
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.517A>G
  hgvsp: ENSP00000433457.1:p.Thr173Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.517A>G
  hgvsp: ENSP00000380861.1:p.Thr173Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.517A>G
  hgvsp: ENSP00000434177.1:p.Thr173Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.506A>G
  hgvsp: ENSP00000436187.1:p.Thr170Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.575A>G
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.517A>G
  hgvsp: ENSP00000350574.4:p.Thr173Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.517A>G
  hgvsp: ENSP00000408079.1:p.Thr173Ala
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.78A>G
  hgvsp: ENSP00000432558.1:p.Thr27Ala
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21951
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5217
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 953
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr173Ala
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-130131252-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131252
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131252
    reference: chr 11
allele count: 1
allele frequency: 8.284592315212168e-6
allele num: 120706
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.517A>C
  hgvsp: ENSP00000434177.1:p.Thr173Pro
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.517A>C
  hgvsp: ENSP00000408079.1:p.Thr173Pro
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.517A>C
  hgvsp: ENSP00000350574.4:p.Thr173Pro
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.506A>C
  hgvsp: ENSP00000436187.1:p.Thr170Pro
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.78A>C
  hgvsp: ENSP00000432558.1:p.Thr27Pro
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.517A>C
  hgvsp: ENSP00000380861.1:p.Thr173Pro
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.575A>C
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.517A>C
  hgvsp: ENSP00000433457.1:p.Thr173Pro
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5217
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21951
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 953
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3781
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1498
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6034
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr173Pro
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/11-130131261-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131261
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131261
    reference: chr 11
allele count: 2
allele frequency: 1.656891009709381e-5
allele num: 120708
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.508G>T
  hgvsp: ENSP00000350574.4:p.Val170Leu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.69G>T
  hgvsp: ENSP00000432558.1:p.Val24Leu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.508G>T
  hgvsp: ENSP00000408079.1:p.Val170Leu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.508G>T
  hgvsp: ENSP00000433457.1:p.Val170Leu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.508G>T
  hgvsp: ENSP00000434177.1:p.Val170Leu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.508G>T
  hgvsp: ENSP00000380861.1:p.Val170Leu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.566G>T
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.497G>T
  hgvsp: ENSP00000436187.1:p.Val167Leu
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 951
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45354
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val170Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
population: Latino
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

11-130131261-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131261
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131261
    reference: chr 11
allele count: 1
allele frequency: 8.284455048546906e-6
allele num: 120708
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.508G>A
  hgvsp: ENSP00000434177.1:p.Val170Ile
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.497G>A
  hgvsp: ENSP00000436187.1:p.Val167Ile
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.508G>A
  hgvsp: ENSP00000380861.1:p.Val170Ile
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.508G>A
  hgvsp: ENSP00000350574.4:p.Val170Ile
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.69G>A
  hgvsp: ENSP00000432558.1:p.Val24Ile
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.566G>A
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.508G>A
  hgvsp: ENSP00000408079.1:p.Val170Ile
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.508G>A
  hgvsp: ENSP00000433457.1:p.Val170Ile
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6027
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val170Ile
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-130131262-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131262
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131262
    reference: chr 11
allele count: 2348
allele frequency: 1.9452867392421e-2
allele num: 120702
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.507G>T
  hgvsp: ENST00000357899.4:c.507G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.68G>T
  hgvsp: ENST00000529982.1:c.68G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.507G>T
  hgvsp: ENST00000530205.1:c.507G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.496G>T
  hgvsp: ENST00000527478.1:c.496G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.507G>T
  hgvsp: ENST00000445008.2:c.507G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.507G>T
  hgvsp: ENST00000397753.1:c.507G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.507G>T
  hgvsp: ENST00000525842.1:c.507G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.565G>T
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4917
  bin: 3.25e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.25e1
  variant carriers: 160
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 3.75e1
  variant carriers: 110
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.75e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 4.25e1
  variant carriers: 148
genotype depth: GenotypeDepth
  all individuals: 26161
  bin: 2.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 327
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 5.75e1
  variant carriers: 191
genotype depth: GenotypeDepth
  all individuals: 21482
  bin: 2.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 178
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 4.75e1
  variant carriers: 185
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.25e1
  variant carriers: 206
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 144
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.75e1
  variant carriers: 215
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5716
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val169Val
num of homozygotes: 78
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

11-130131266-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131266
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131266
    reference: chr 11
allele count: 1
allele frequency: 8.284180528862085e-6
allele num: 120712
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.64G>C
  hgvsp: ENSP00000432558.1:p.Ser22Thr
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.561G>C
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.503G>C
  hgvsp: ENSP00000350574.4:p.Ser168Thr
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.503G>C
  hgvsp: ENSP00000408079.1:p.Ser168Thr
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.503G>C
  hgvsp: ENSP00000434177.1:p.Ser168Thr
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.503G>C
  hgvsp: ENSP00000433457.1:p.Ser168Thr
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.503G>C
  hgvsp: ENSP00000380861.1:p.Ser168Thr
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.492G>C
  hgvsp: ENSP00000436187.1:p.Ser165Thr
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1348
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser168Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP

11-130131271-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131271
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131271
    reference: chr 11
allele count: 11
allele frequency: 9.112749565073317e-5
allele num: 120710
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.498G>C
  hgvsp: ENSP00000434177.1:p.Glu166Asp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.556G>C
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.498G>C
  hgvsp: ENSP00000350574.4:p.Glu166Asp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.498G>C
  hgvsp: ENSP00000408079.1:p.Glu166Asp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.498G>C
  hgvsp: ENSP00000433457.1:p.Glu166Asp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.59G>C
  hgvsp: ENSP00000432558.1:p.Glu20Asp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.487G>C
  hgvsp: ENSP00000436187.1:p.Glu163Asp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.498G>C
  hgvsp: ENSP00000380861.1:p.Glu166Asp
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6030
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu166Asp
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: C
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-130131271-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131271
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131271
    reference: chr 11
allele count: 1
allele frequency: 8.284317786430287e-6
allele num: 120710
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.498G>A
  hgvsp: ENST00000445008.2:c.498G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.498G>A
  hgvsp: ENST00000525842.1:c.498G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.556G>A
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.498G>A
  hgvsp: ENST00000397753.1:c.498G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.498G>A
  hgvsp: ENST00000530205.1:c.498G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.498G>A
  hgvsp: ENST00000357899.4:c.498G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.59G>A
  hgvsp: ENST00000529982.1:c.59G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.487G>A
  hgvsp: ENST00000527478.1:c.487G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1408
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3477
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 837
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu166Glu
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

11-130131275-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131275
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131275
    reference: chr 11
allele count: 1
allele frequency: 8.284180528862085e-6
allele num: 120712
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.494C>T
  hgvsp: ENSP00000434177.1:p.Ser165Leu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.494C>T
  hgvsp: ENSP00000408079.1:p.Ser165Leu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.483C>T
  hgvsp: ENSP00000436187.1:p.Ser162Leu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.55C>T
  hgvsp: ENSP00000432558.1:p.Ser19Leu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.494C>T
  hgvsp: ENSP00000433457.1:p.Ser165Leu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.494C>T
  hgvsp: ENSP00000380861.1:p.Ser165Leu
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.552C>T
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.494C>T
  hgvsp: ENSP00000350574.4:p.Ser165Leu
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser165Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD

11-130131277-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131277
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131277
    reference: chr 11
allele count: 1
allele frequency: 8.284043275842073e-6
allele num: 120714
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.492C>T
  hgvsp: ENST00000530205.1:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.492C>T
  hgvsp: ENST00000445008.2:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.492C>T
  hgvsp: ENST00000357899.4:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.550C>T
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.492C>T
  hgvsp: ENST00000397753.1:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.481C>T
  hgvsp: ENST00000527478.1:c.481C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.53C>T
  hgvsp: ENST00000529982.1:c.53C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.492C>T
  hgvsp: ENST00000525842.1:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3467
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1345
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser164Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum

11-130131283-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131283
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131283
    reference: chr 11
allele count: 385
allele frequency: 3.190096614354606e-3
allele num: 120686
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.544C>T
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.486C>T
  hgvsp: ENST00000530205.1:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.486C>T
  hgvsp: ENST00000445008.2:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.486C>T
  hgvsp: ENST00000525842.1:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.47C>T
  hgvsp: ENST00000529982.1:c.47C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.475C>T
  hgvsp: ENST00000527478.1:c.475C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.486C>T
  hgvsp: ENST00000397753.1:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.486C>T
  hgvsp: ENST00000357899.4:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 9.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 26430
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.75e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 5171
  bin: 3.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 22586
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 3.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 35
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro162Pro
num of homozygotes: 1
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum

11-130131298-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131298
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131298
    reference: chr 11
allele count: 4
allele frequency: 3.313836926084867e-5
allele num: 120706
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.529T>C
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.32T>C
  hgvsp: ENST00000529982.1:c.32T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.471T>C
  hgvsp: ENST00000357899.4:c.471T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.471T>C
  hgvsp: ENST00000530205.1:c.471T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.471T>C
  hgvsp: ENST00000445008.2:c.471T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.471T>C
  hgvsp: ENST00000525842.1:c.471T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.460T>C
  hgvsp: ENST00000527478.1:c.460T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.471T>C
  hgvsp: ENST00000397753.1:c.471T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22837
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46249
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp157Asp
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

11-130131300-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131300
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131300
    reference: chr 11
allele count: 1
allele frequency: 8.284592315212168e-6
allele num: 120706
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.527G>A
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.458G>A
  hgvsp: ENSP00000436187.1:p.Asp154Asn
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.469G>A
  hgvsp: ENSP00000380861.1:p.Asp157Asn
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.469G>A
  hgvsp: ENSP00000350574.4:p.Asp157Asn
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.469G>A
  hgvsp: ENSP00000433457.1:p.Asp157Asn
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.30G>A
  hgvsp: ENSP00000432558.1:p.Asp11Asn
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.469G>A
  hgvsp: ENSP00000434177.1:p.Asp157Asn
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.469G>A
  hgvsp: ENSP00000408079.1:p.Asp157Asn
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22828
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26433
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp157Asn
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

11-130131302-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131302
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131302
    reference: chr 11
allele count: 1
allele frequency: 8.285278716776033e-6
allele num: 120696
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.28G>A
  hgvsp: ENSP00000432558.1:p.Arg10Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.467G>A
  hgvsp: ENSP00000408079.1:p.Arg156Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.456G>A
  hgvsp: ENSP00000436187.1:p.Arg153Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.467G>A
  hgvsp: ENSP00000350574.4:p.Arg156Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.467G>A
  hgvsp: ENSP00000380861.1:p.Arg156Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.467G>A
  hgvsp: ENSP00000433457.1:p.Arg156Gln
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.525G>A
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.467G>A
  hgvsp: ENSP00000434177.1:p.Arg156Gln
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1317
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg156Gln
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

11-130131317-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131317
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131317
    reference: chr 11
allele count: 2
allele frequency: 1.657028285472833e-5
allele num: 120698
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.452G>A
  hgvsp: ENSP00000350574.4:p.Cys151Tyr
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.452G>A
  hgvsp: ENSP00000434177.1:p.Cys151Tyr
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.13G>A
  hgvsp: ENSP00000432558.1:p.Cys5Tyr
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.452G>A
  hgvsp: ENSP00000433457.1:p.Cys151Tyr
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.452G>A
  hgvsp: ENSP00000408079.1:p.Cys151Tyr
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.452G>A
  hgvsp: ENSP00000380861.1:p.Cys151Tyr
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.441G>A
  hgvsp: ENSP00000436187.1:p.Cys148Tyr
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.510G>A
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22859
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1307
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Cys151Tyr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

11-130131323-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131323
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131323
    reference: chr 11
allele count: 1
allele frequency: 8.285553309249991e-6
allele num: 120692
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.504C>G
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.446C>G
  hgvsp: ENSP00000380861.1:p.Ser149Cys
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.446C>G
  hgvsp: ENSP00000350574.4:p.Ser149Cys
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.446C>G
  hgvsp: ENSP00000408079.1:p.Ser149Cys
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.446C>G
  hgvsp: ENSP00000434177.1:p.Ser149Cys
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.446C>G
  hgvsp: ENSP00000433457.1:p.Ser149Cys
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000432558
  ensembl transcript: ENST00000529982
  gene symbol: ZBTB44
  hgvsc: ENST00000529982.1:c.7C>G
  hgvsp: ENSP00000432558.1:p.Ser3Cys
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.435C>G
  hgvsp: ENSP00000436187.1:p.Ser146Cys
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22865
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26430
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5213
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1380
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46431
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser149Cys
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: QD

11-130131330-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130131330
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 130131330
    reference: chr 11
allele count: 1
allele frequency: 8.2847295864263e-6
allele num: 120704
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000408079
  ensembl transcript: ENST00000445008
  gene symbol: ZBTB44
  hgvsc: ENST00000445008.2:c.439A>G
  hgvsp: ENSP00000408079.1:p.Asn147Asp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000436187
  ensembl transcript: ENST00000527478
  gene symbol: ZBTB44
  hgvsc: ENST00000527478.1:c.428A>G
  hgvsp: ENSP00000436187.1:p.Asn144Asp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196323
  ensembl transcript: ENST00000529348
  gene symbol: ZBTB44
  hgvsc: ENST00000529348.1:n.497A>G
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000380861
  ensembl transcript: ENST00000397753
  gene symbol: ZBTB44
  hgvsc: ENST00000397753.1:c.439A>G
  hgvsp: ENSP00000380861.1:p.Asn147Asp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000433457
  ensembl transcript: ENST00000525842
  gene symbol: ZBTB44
  hgvsc: ENST00000525842.1:c.439A>G
  hgvsp: ENSP00000433457.1:p.Asn147Asp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000350574
  ensembl transcript: ENST00000357899
  gene symbol: ZBTB44
  hgvsc: ENST00000357899.4:c.439A>G
  hgvsp: ENSP00000350574.4:p.Asn147Asp
  variant of: http://identifiers.org/hgnc/25001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196323
  ensembl protein: ENSP00000434177
  ensembl transcript: ENST00000530205
  gene symbol: ZBTB44
  hgvsc: ENST00000530205.1:c.439A>G
  hgvsp: ENSP00000434177.1:p.Asn147Asp
  variant of: http://identifiers.org/hgnc/25001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5215
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asn147Asp
num of homozygotes: 0
reference allele: T

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

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1527
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 974
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45029
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4209
bin: 9.75e1
variant carriers: 449

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1488
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 31
allele frequency: 2.677954388389772e-3
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.990380293086398e-5
allele num: 66738
num of homozygotes: 0

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

African
type: Population
allele count: 423
allele frequency: 4.316326530612245e-2
allele num: 9800
num of homozygotes: 12

Other
type: Population
allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.96e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.95e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.13e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.12e0

QD
type: SiteQuality
SIO_000300: 1.57e1

DP
type: SiteQuality
SIO_000300: 1.744179e6

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

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

GenotypeQuality
all individuals: 14
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 443
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 985
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45276
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1551
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6146
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 9.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.672397e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.335e0

MQRankSum
type: SiteQuality
SIO_000300: 8.22e-1

FS
type: SiteQuality
SIO_000300: 6.464e0

MQ
type: SiteQuality
SIO_000300: 5.917e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.611e0

VQSLOD
type: SiteQuality
SIO_000300: -6.506999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.34e0

QD
type: SiteQuality
SIO_000300: 1.463e1

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

GenotypeQuality
all individuals: 985
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45264
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1551
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3821
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.672268e6

QD
type: SiteQuality
SIO_000300: 1.489e1

MQRankSum
type: SiteQuality
SIO_000300: -1.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.457e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.23e-1

MQ
type: SiteQuality
SIO_000300: 5.986e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.77e-1

FS
type: SiteQuality
SIO_000300: 3.469e0

VQSLOD
type: SiteQuality
SIO_000300: 9.419999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

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

GenotypeQuality
all individuals: 442
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1551
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1503
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3820
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 45267
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 985
bin: 8.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQ
type: SiteQuality
SIO_000300: 5.976e1

MQRankSum
type: SiteQuality
SIO_000300: -8.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.017e0

FS
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.32e-1

VQSLOD
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DP
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QD
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SIO_000300: 1.63e1

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

GenotypeQuality
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variant carriers: 0

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

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

European (Finnish)
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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: 898
num of homozygotes: 0

African
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allele frequency: 1.021033285685113e-4
allele num: 9794
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South Asian
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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VQSLOD
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FS
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SIO_000300: 9.09e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

InbreedingCoeff
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SIO_000300: 1.9e-3

ClippingRankSum
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DP
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.88e-1

MQRankSum
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
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allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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ReadPosRankSum
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SIO_000300: 9.55e-1

BaseQRankSum
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ClippingRankSum
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MQRankSum
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DP
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FS
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 3.0e-4

MQ
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SIO_000300: 6.0e1

VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5.75e1
variant carriers: 0

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

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

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

South Asian
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allele num: 16510
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
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SIO_000300: 1.1e-2

ReadPosRankSum
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.580000000000001e-1

FS
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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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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 1
allele frequency: 1.021659174499387e-4
allele num: 9788
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
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.524e0

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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DP
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MQ
type: SiteQuality
SIO_000300: 5.892e1

ClippingRankSum
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ReadPosRankSum
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QD
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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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variant carriers: 0

East Asian
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num of homozygotes: 0

African
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European (Finnish)
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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 frequency: 1.049223574554829e-4
allele num: 66716
num of homozygotes: 0

Latino
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Other
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South Asian
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InbreedingCoeff
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BaseQRankSum
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QD
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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MQ
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DP
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VQSLOD
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

East Asian
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Other
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African
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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DP
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VQSLOD
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InbreedingCoeff
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MQ
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FS
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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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Other
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African
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Latino
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European (Finnish)
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South Asian
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European (Non-Finnish)
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allele num: 66702
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East Asian
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BaseQRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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FS
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MQ
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ClippingRankSum
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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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Latino
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Finnish)
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allele num: 6614
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European (Non-Finnish)
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allele num: 66702
num of homozygotes: 0

East Asian
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Other
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South Asian
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InbreedingCoeff
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ClippingRankSum
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MQ
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QD
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MQRankSum
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VQSLOD
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DP
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BaseQRankSum
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FS
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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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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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InbreedingCoeff
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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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BaseQRankSum
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ReadPosRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

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

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

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

Latino
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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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East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.499700059988002e-5
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VQSLOD
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BaseQRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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QD
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MQ
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
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num of homozygotes: 0

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

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: 4.5004500450045e-5
allele num: 66660
num of homozygotes: 0

Other
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VQSLOD
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ReadPosRankSum
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FS
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BaseQRankSum
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DP
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ClippingRankSum
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MQ
type: SiteQuality
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MQRankSum
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QD
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InbreedingCoeff
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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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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European (Non-Finnish)
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allele frequency: 1.5001500150015e-5
allele num: 66660
num of homozygotes: 0

East Asian
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South Asian
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ClippingRankSum
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VQSLOD
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MQ
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MQRankSum
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FS
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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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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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European (Finnish)
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num of homozygotes: 0

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

European (Non-Finnish)
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Other
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Latino
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European (Finnish)
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allele num: 6612
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East Asian
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South Asian
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QD
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MQRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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DP
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ClippingRankSum
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FS
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66662
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African
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East Asian
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Latino
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European (Finnish)
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Other
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South Asian
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FS
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VQSLOD
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ReadPosRankSum
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MQ
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BaseQRankSum
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QD
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MQRankSum
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ClippingRankSum
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DP
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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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African
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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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num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.325e1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.38e-1

FS
type: SiteQuality
SIO_000300: 3.736e0

MQRankSum
type: SiteQuality
SIO_000300: 8.62e-1

DP
type: SiteQuality
SIO_000300: 1.666435e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.239e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.57e-1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 34

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 44796
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.501530520376928e-5
allele num: 66644
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
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: 9736
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 31
allele frequency: 3.599628425452857e-3
allele num: 8612
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.971e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.14e-1

FS
type: SiteQuality
SIO_000300: 1.218e0

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-2

QD
type: SiteQuality
SIO_000300: 1.247e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.446e0

DP
type: SiteQuality
SIO_000300: 1.667945e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.77e-1

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.108463434675431e-4
allele num: 9736
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66644
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.971e1

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-2

FS
type: SiteQuality
SIO_000300: 1.218e0

QD
type: SiteQuality
SIO_000300: 1.247e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.446e0

VQSLOD
type: SiteQuality
SIO_000300: 4.13e0

DP
type: SiteQuality
SIO_000300: 1.667945e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.14e-1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3800
bin: 9.75e1
variant carriers: 1

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.026904908605463e-4
allele num: 9738
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

DP
type: SiteQuality
SIO_000300: 1.66599e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 6.431e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.39e0

QD
type: SiteQuality
SIO_000300: 1.575e1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3800
bin: 9.75e1
variant carriers: 1

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

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9742
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 8.120000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.666006e6

VQSLOD
type: SiteQuality
SIO_000300: 3.76e-1

MQ
type: SiteQuality
SIO_000300: 5.949e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.393e0

QD
type: SiteQuality
SIO_000300: 1.417e1

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 442
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GenotypeQuality
all individuals: 1530
bin: 7.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66638
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.039e0

DP
type: SiteQuality
SIO_000300: 1.66553e6

MQRankSum
type: SiteQuality
SIO_000300: 3.57e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.34e-1

QD
type: SiteQuality
SIO_000300: 1.332e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
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: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9744
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.0016509079994e-5
allele num: 66630
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.45e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.796e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.29e0

MQRankSum
type: SiteQuality
SIO_000300: 1.85e0

DP
type: SiteQuality
SIO_000300: 1.666144e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-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
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bin: 7.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.162520344106022e-4
allele num: 8602
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9742
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.37e-1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
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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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500690317546071e-5
allele num: 66636
num of homozygotes: 0

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

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

East Asian
type: Population
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
allele num: 11550
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

MQ
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.667799e6

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 49

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9766
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 34
allele frequency: 5.100969184144988e-4
allele num: 66654
num of homozygotes: 0

Latino
type: Population
allele count: 15
allele frequency: 1.298701298701299e-3
allele num: 11550
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.85e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.266e1

VQSLOD
type: SiteQuality
SIO_000300: 4.97e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.105e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.15e-1

DP
type: SiteQuality
SIO_000300: 1.670241e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

MQ
type: SiteQuality
SIO_000300: 5.982e1

GenotypeQuality
all individuals: 139
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44623
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 2.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499970000599988e-5
allele num: 66668
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.52e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.26e-1

DP
type: SiteQuality
SIO_000300: 1.670207e6

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.499910001799964e-5
allele num: 66668
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.52e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.18e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.91e-1

DP
type: SiteQuality
SIO_000300: 1.670207e6

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 15

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 63
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.249347689170141e-4
allele num: 66686
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.672716e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.261e0

FS
type: SiteQuality
SIO_000300: 1.16e0

QD
type: SiteQuality
SIO_000300: 1.408e1

VQSLOD
type: SiteQuality
SIO_000300: 3.99e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.01e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 37

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 31
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GenotypeQuality
all individuals: 57
bin: 5.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 37
allele frequency: 4.300325430032543e-3
allele num: 8604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.226e1

FS
type: SiteQuality
SIO_000300: 1.137e0

VQSLOD
type: SiteQuality
SIO_000300: 2.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.55e0

DP
type: SiteQuality
SIO_000300: 1.673476e6

MQRankSum
type: SiteQuality
SIO_000300: 1.6e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.12e-1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 6056
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
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: 898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999040307101727e-5
allele num: 66688
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.277e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.05e-1

FS
type: SiteQuality
SIO_000300: 3.585e0

MQRankSum
type: SiteQuality
SIO_000300: -2.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.64e-1

DP
type: SiteQuality
SIO_000300: 1.673158e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.053268765133172e-4
allele num: 6608
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.75e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.04e0

MQRankSum
type: SiteQuality
SIO_000300: 7.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.95e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

QD
type: SiteQuality
SIO_000300: 1.369e1

DP
type: SiteQuality
SIO_000300: 1.673551e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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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bin: 3.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9784
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999310158663508e-5
allele num: 66682
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
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: 898
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.673522e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.952e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

FS
type: SiteQuality
SIO_000300: 2.478e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.37e0

QD
type: SiteQuality
SIO_000300: 1.603e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

VQSLOD
type: SiteQuality
SIO_000300: 7.25e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 50
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GenotypeQuality
all individuals: 432
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.161170459823502e-4
allele num: 8612
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9784
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.81e0

FS
type: SiteQuality
SIO_000300: 2.955e0

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.973e1

MQRankSum
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SIO_000300: -1.449e0

DP
type: SiteQuality
SIO_000300: 1.673803e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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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: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1526
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45033
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9782
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.07e-1

FS
type: SiteQuality
SIO_000300: 1.0296e1

MQ
type: SiteQuality
SIO_000300: 5.963e1

MQRankSum
type: SiteQuality
SIO_000300: 1.0e0

DP
type: SiteQuality
SIO_000300: 1.673769e6

VQSLOD
type: SiteQuality
SIO_000300: -6.608000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.029e0

QD
type: SiteQuality
SIO_000300: 1.297e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.17e-1

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6061
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9782
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 8.38e-1

MQ
type: SiteQuality
SIO_000300: 5.924e1

DP
type: SiteQuality
SIO_000300: 1.674416e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.191e0

FS
type: SiteQuality
SIO_000300: 4.533e0

VQSLOD
type: SiteQuality
SIO_000300: -3.557e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.62e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.49e-1

QD
type: SiteQuality
SIO_000300: 1.352e1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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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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bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66700
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: 898
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9778
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.314e1

MQ
type: SiteQuality
SIO_000300: 5.925e1

FS
type: SiteQuality
SIO_000300: 5.738e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.681e0

VQSLOD
type: SiteQuality
SIO_000300: -1.016e0

MQRankSum
type: SiteQuality
SIO_000300: 2.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.62e-1

DP
type: SiteQuality
SIO_000300: 1.674328e6

GenotypeQuality
all individuals: 8
bin: 1.75e1
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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49947518368571e-5
allele num: 66690
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.538e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.755e0

QD
type: SiteQuality
SIO_000300: 1.312e1

MQRankSum
type: SiteQuality
SIO_000300: -3.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.32e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.89e-1

DP
type: SiteQuality
SIO_000300: 1.674257e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 17
bin: 5.75e1
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GenotypeQuality
all individuals: 60
bin: 3.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.376e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.8e-1

DP
type: SiteQuality
SIO_000300: 1.674221e6

VQSLOD
type: SiteQuality
SIO_000300: 6.31e-1

QD
type: SiteQuality
SIO_000300: 1.357e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.81e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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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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: 45062
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 1.022494887525562e-4
allele num: 9780
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.674285e6

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.08e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

MQRankSum
type: SiteQuality
SIO_000300: 1.82e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.66e0

GenotypeQuality
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bin: 4.25e1
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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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: 6

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9782
num of homozygotes: 0

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

East Asian
type: Population
allele count: 6
allele frequency: 6.970260223048327e-4
allele num: 8608
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.674849e6

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.095e0

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -5.9e-2

QD
type: SiteQuality
SIO_000300: 1.088e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.38e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9784
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49947518368571e-5
allele num: 66690
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.582e1

VQSLOD
type: SiteQuality
SIO_000300: -6.121e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 428
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variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1452
bin: 7.75e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9784
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.81e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.258e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.77e0

DP
type: SiteQuality
SIO_000300: 1.675178e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ClippingRankSum
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SIO_000300: -1.691e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.32e0

QD
type: SiteQuality
SIO_000300: 1.201e1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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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: 5.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.98e-1

DP
type: SiteQuality
SIO_000300: 1.675344e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.132e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.02e-1

VQSLOD
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SIO_000300: 5.74e-1

ClippingRankSum
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SIO_000300: -8.0e-3

InbreedingCoeff
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SIO_000300: 2.4e-3

QD
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SIO_000300: 1.453e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e-2

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.99895036737142e-5
allele num: 66690
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.974e1

DP
type: SiteQuality
SIO_000300: 1.675438e6

QD
type: SiteQuality
SIO_000300: 1.258e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

VQSLOD
type: SiteQuality
SIO_000300: 4.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.2e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.032e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

FS
type: SiteQuality
SIO_000300: 1.201e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.498275396658768e-5
allele num: 66682
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

European (Finnish)
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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: 16506
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.64e0

QD
type: SiteQuality
SIO_000300: 1.416e1

MQRankSum
type: SiteQuality
SIO_000300: 1.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.09e-1

MQ
type: SiteQuality
SIO_000300: 5.93e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 5.21e-1

DP
type: SiteQuality
SIO_000300: 1.675858e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e-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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9788
num of homozygotes: 0

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

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.677769e6

MQRankSum
type: SiteQuality
SIO_000300: 1.46e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

VQSLOD
type: SiteQuality
SIO_000300: 2.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.27e-1

FS
type: SiteQuality
SIO_000300: 3.397e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.213e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

QD
type: SiteQuality
SIO_000300: 1.238e1

GenotypeQuality
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bin: 5.75e1
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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variant carriers: 2

GenotypeQuality
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variant carriers: 0

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.321262766945218e-4
allele num: 8616
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66704
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.033e0

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.488e0

BaseQRankSum
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SIO_000300: -1.82e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.967e1

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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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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variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 3.612e0

QD
type: SiteQuality
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ClippingRankSum
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DP
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.963e1

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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bin: 6.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

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

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

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

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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MQ
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MQRankSum
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FS
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DP
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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ClippingRankSum
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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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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 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: 11560
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.217e0

DP
type: SiteQuality
SIO_000300: 1.678838e6

VQSLOD
type: SiteQuality
SIO_000300: 5.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.46e0

MQRankSum
type: SiteQuality
SIO_000300: 9.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.4e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.1e-3

GenotypeQuality
all individuals: 1496
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6027
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3783
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 58
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
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: 898
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.944e1

MQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.4e-1

DP
type: SiteQuality
SIO_000300: 1.679057e6

FS
type: SiteQuality
SIO_000300: 4.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.569e0

VQSLOD
type: SiteQuality
SIO_000300: 7.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

QD
type: SiteQuality
SIO_000300: 1.153e1

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

GenotypeQuality
all individuals: 46
bin: 7.5e0
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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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3783
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

QD
type: SiteQuality
SIO_000300: 1.153e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.569e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

DP
type: SiteQuality
SIO_000300: 1.679057e6

MQ
type: SiteQuality
SIO_000300: 5.944e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.4e-1

FS
type: SiteQuality
SIO_000300: 4.93e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.45e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.28e-1

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1279
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 54
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variant carriers: 0

GenotypeQuality
all individuals: 1343
bin: 7.25e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
all individuals: 5541
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variant carriers: 2260

GenotypeQuality
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bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 44607
bin: 6.25e1
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GenotypeQuality
all individuals: 784
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variant carriers: 1

GenotypeQuality
all individuals: 358
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variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 109
allele frequency: 6.60205935796487e-3
allele num: 16510
num of homozygotes: 3

Other
type: Population
allele count: 16
allele frequency: 1.78173719376392e-2
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 843
allele frequency: 1.263564961928173e-2
allele num: 66716
num of homozygotes: 5

African
type: Population
allele count: 1191
allele frequency: 1.21605064325097e-1
allele num: 9794
num of homozygotes: 68

East Asian
type: Population
allele count: 1
allele frequency: 1.160092807424594e-4
allele num: 8620
num of homozygotes: 0

Latino
type: Population
allele count: 179
allele frequency: 1.548978885427484e-2
allele num: 11556
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 9
allele frequency: 1.361985472154964e-3
allele num: 6608
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.29e0

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.22e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

QD
type: SiteQuality
SIO_000300: 1.377e1

DP
type: SiteQuality
SIO_000300: 1.76029e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.57e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.25e0

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46142
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variant carriers: 0

GenotypeQuality
all individuals: 31
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GenotypeQuality
all individuals: 839
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 519
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GenotypeQuality
all individuals: 51
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GenotypeQuality
all individuals: 376
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GenotypeQuality
all individuals: 17
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GenotypeQuality
all individuals: 36
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GenotypeQuality
all individuals: 1410
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6031
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3469
bin: 9.75e1
variant carriers: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.831e1

VQSLOD
type: SiteQuality
SIO_000300: -1.944e0

MQRankSum
type: SiteQuality
SIO_000300: -4.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.968e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

FS
type: SiteQuality
SIO_000300: 3.363e0

QD
type: SiteQuality
SIO_000300: 1.161e1

DP
type: SiteQuality
SIO_000300: 1.678343e6

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

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46148
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1349
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variant carriers: 0

GenotypeQuality
all individuals: 40
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 17
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GenotypeQuality
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GenotypeQuality
all individuals: 3477
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1408
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variant carriers: 0

GenotypeQuality
all individuals: 520
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variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.648829331174866e-4
allele num: 66714
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.120000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.507e1

DP
type: SiteQuality
SIO_000300: 1.678711e6

FS
type: SiteQuality
SIO_000300: 1.74e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.05e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.2e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.29e-1

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

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

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 47
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variant carriers: 0

GenotypeQuality
all individuals: 53
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 6030
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GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 375
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variant carriers: 0

GenotypeQuality
all individuals: 520
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variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46148
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1349
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.021033285685113e-4
allele num: 9794
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
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: 898
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.66e-1

FS
type: SiteQuality
SIO_000300: 1.74e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.120000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.05e-1

DP
type: SiteQuality
SIO_000300: 1.678711e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.29e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

QD
type: SiteQuality
SIO_000300: 1.507e1

GenotypeQuality
all individuals: 1407
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6013
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variant carriers: 0

GenotypeQuality
all individuals: 23
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 46061
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41
bin: 7.5e0
variant carriers: 0

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 6.29e-1

FS
type: SiteQuality
SIO_000300: 8.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.393e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.93e-1

DP
type: SiteQuality
SIO_000300: 1.678126e6

MQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.200000000000001e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.76e0

QD
type: SiteQuality
SIO_000300: 2.493e1

GenotypeQuality
all individuals: 45
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
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GenotypeQuality
all individuals: 6020
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1406
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variant carriers: 0

GenotypeQuality
all individuals: 60
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variant carriers: 0

GenotypeQuality
all individuals: 46102
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GenotypeQuality
all individuals: 57
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variant carriers: 0

GenotypeQuality
all individuals: 44
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GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 20
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GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 372
bin: 8.75e1
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GenotypeQuality
all individuals: 836
bin: 8.25e1
variant carriers: 0

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.020616452337212e-4
allele num: 9798
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.95e-1

QD
type: SiteQuality
SIO_000300: 7.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.18e0

MQRankSum
type: SiteQuality
SIO_000300: 2.21e-1

MQ
type: SiteQuality
SIO_000300: 5.924e1

VQSLOD
type: SiteQuality
SIO_000300: -3.126e-1

DP
type: SiteQuality
SIO_000300: 1.678146e6

FS
type: SiteQuality
SIO_000300: 3.176e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e-1

GenotypeQuality
all individuals: 809
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3626
bin: 9.75e1
variant carriers: 384

GenotypeQuality
all individuals: 41
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1309
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1373
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5982
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46060
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 5
allele frequency: 5.567928730512249e-3
allele num: 898
num of homozygotes: 0

Latino
type: Population
allele count: 75
allele frequency: 6.490134994807892e-3
allele num: 11556
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.801810164771409e-4
allele num: 8618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 12
allele frequency: 1.815980629539952e-3
allele num: 6608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 283
allele frequency: 4.24287856071964e-3
allele num: 66700
num of homozygotes: 1

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

African
type: Population
allele count: 5
allele frequency: 5.104124132298898e-4
allele num: 9796
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.686459e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.49e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.85e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.4e-2

MQ
type: SiteQuality
SIO_000300: 5.971e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.424e1

MQRankSum
type: SiteQuality
SIO_000300: 3.29e-1

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

GenotypeQuality
all individuals: 68
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1394
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6013
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3271
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 813
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1313
bin: 7.75e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.99610253335332e-5
allele num: 66710
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.134e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 7.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.35e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

QD
type: SiteQuality
SIO_000300: 1.194e1

VQSLOD
type: SiteQuality
SIO_000300: 1.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.43e-1

DP
type: SiteQuality
SIO_000300: 1.672271e6

MQRankSum
type: SiteQuality
SIO_000300: 3.69e-1

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

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1395
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 814
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3269
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6006
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46235
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 360
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1313
bin: 7.75e1
variant carriers: 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: 898
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.62e0

DP
type: SiteQuality
SIO_000300: 1.672075e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.629e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

MQ
type: SiteQuality
SIO_000300: 5.942e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.79e-1

QD
type: SiteQuality
SIO_000300: 1.224e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

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

GenotypeQuality
all individuals: 61
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6000
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3269
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1388
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 815
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46240
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66704
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.68e-1

QD
type: SiteQuality
SIO_000300: 1.461e1

MQRankSum
type: SiteQuality
SIO_000300: -4.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

MQ
type: SiteQuality
SIO_000300: 5.936e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.19e-1

DP
type: SiteQuality
SIO_000300: 1.672354e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

GenotypeQuality
all individuals: 820
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46404
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1384
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3269
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5983
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
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: 66706
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159823706796567e-4
allele num: 8622
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 1.02082482645978e-4
allele num: 9796
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.899999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.95e-2

QD
type: SiteQuality
SIO_000300: 1.246e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.083e0

MQRankSum
type: SiteQuality
SIO_000300: -4.35e-1

DP
type: SiteQuality
SIO_000300: 1.67265e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.988e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

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

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

GenotypeQuality
all individuals: 1298
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5990
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 50
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3265
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 358
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

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

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.87e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.856e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.67265e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.399e1