18-45567412-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567412
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567412
    reference: chr 18
allele count: 1
allele frequency: 8.284455048546906e-6
allele num: 120708
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.67A>G
  hgvsp: ENSP00000465265.1:p.Ser23Gly
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000439781
  ensembl transcript: ENST00000535628
  gene symbol: ZBTB7C
  hgvsc: ENST00000535628.2:c.67A>G
  hgvsp: ENSP00000439781.1:p.Ser23Gly
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.67A>G
  hgvsp: ENSP00000468502.1:p.Ser23Gly
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.67A>G
  hgvsp: ENSP00000468019.1:p.Ser23Gly
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.67A>G
  hgvsp: ENSP00000468537.1:p.Ser23Gly
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.67A>G
  hgvsp: ENSP00000465760.1:p.Ser23Gly
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.67A>G
  hgvsp: ENSP00000468306.1:p.Ser23Gly
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.67A>G
  hgvsp: ENSP00000468782.1:p.Ser23Gly
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.67A>G
  hgvsp: ENSP00000468087.1:p.Ser23Gly
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000328732
  ensembl transcript: ENST00000332053
  gene symbol: ZBTB7C
  hgvsc: ENST00000332053.2:c.67A>G
  hgvsp: ENSP00000328732.2:p.Ser23Gly
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467323
  ensembl transcript: ENST00000590437
  gene symbol: ZBTB7C
  hgvsc: ENST00000590437.1:c.67A>G
  hgvsp: ENSP00000467323.1:p.Ser23Gly
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.67A>G
  hgvsp: ENSP00000465835.1:p.Ser23Gly
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.67A>G
  hgvsp: ENSP00000467877.1:p.Ser23Gly
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.67A>G
  hgvsp: ENSP00000468254.1:p.Ser23Gly
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.67A>G
  hgvsp: ENSP00000468659.1:p.Ser23Gly
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.67A>G
  hgvsp: ENSP00000464724.1:p.Ser23Gly
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.67A>G
  hgvsp: ENSP00000467147.1:p.Ser23Gly
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.67A>G
  hgvsp: ENSP00000466006.1:p.Ser23Gly
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser23Gly
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

18-45567422-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567422
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567422
    reference: chr 18
allele count: 1
allele frequency: 8.311170212765958e-6
allele num: 120320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.57G>A
  hgvsp: ENST00000589077.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.57G>A
  hgvsp: ENST00000591279.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.57G>A
  hgvsp: ENST00000590800.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.57G>A
  hgvsp: ENST00000590855.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.57G>A
  hgvsp: ENST00000589619.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000439781
  ensembl transcript: ENST00000535628
  gene symbol: ZBTB7C
  hgvsc: ENST00000535628.2:c.57G>A
  hgvsp: ENST00000535628.2:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.57G>A
  hgvsp: ENST00000585404.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.57G>A
  hgvsp: ENST00000588982.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467323
  ensembl transcript: ENST00000590437
  gene symbol: ZBTB7C
  hgvsc: ENST00000590437.1:c.57G>A
  hgvsp: ENST00000590437.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.57G>A
  hgvsp: ENST00000588970.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.57G>A
  hgvsp: ENST00000592656.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.57G>A
  hgvsp: ENST00000586525.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.57G>A
  hgvsp: ENST00000586438.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.57G>A
  hgvsp: ENST00000589194.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.57G>A
  hgvsp: ENST00000587107.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.57G>A
  hgvsp: ENST00000592387.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000328732
  ensembl transcript: ENST00000332053
  gene symbol: ZBTB7C
  hgvsc: ENST00000332053.2:c.57G>A
  hgvsp: ENST00000332053.2:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.57G>A
  hgvsp: ENST00000586743.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: synonymous
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 9563
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu19Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum

18-45567425-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567425
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567425
    reference: chr 18
allele count: 1
allele frequency: 8.324592511196577e-6
allele num: 120126
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.54T>C
  hgvsp: ENST00000587107.1:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.54T>C
  hgvsp: ENST00000588970.1:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.54T>C
  hgvsp: ENST00000586743.1:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.54T>C
  hgvsp: ENST00000589077.1:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.54T>C
  hgvsp: ENST00000586438.1:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000439781
  ensembl transcript: ENST00000535628
  gene symbol: ZBTB7C
  hgvsc: ENST00000535628.2:c.54T>C
  hgvsp: ENST00000535628.2:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.54T>C
  hgvsp: ENST00000586047.1:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.54T>C
  hgvsp: ENST00000589194.1:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.54T>C
  hgvsp: ENST00000591405.1:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.54T>C
  hgvsp: ENST00000586525.1:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.54T>C
  hgvsp: ENST00000589619.1:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.54T>C
  hgvsp: ENST00000588982.1:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.54T>C
  hgvsp: ENST00000590855.1:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.54T>C
  hgvsp: ENST00000590178.1:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.54T>C
  hgvsp: ENST00000592656.1:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.54T>C
  hgvsp: ENST00000591279.1:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.54T>C
  hgvsp: ENST00000592387.1:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.54T>C
  hgvsp: ENST00000585404.1:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.54T>C
  hgvsp: ENST00000588149.1:c.54T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser18Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

18-45567431-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567431
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567431
    reference: chr 18
allele count: 10
allele frequency: 8.35826883535882e-5
allele num: 119642
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.48C>T
  hgvsp: ENST00000591405.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000439781
  ensembl transcript: ENST00000535628
  gene symbol: ZBTB7C
  hgvsc: ENST00000535628.2:c.48C>T
  hgvsp: ENST00000535628.2:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.48C>T
  hgvsp: ENST00000589077.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.48C>T
  hgvsp: ENST00000588982.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.48C>T
  hgvsp: ENST00000589194.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.48C>T
  hgvsp: ENST00000588970.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.48C>T
  hgvsp: ENST00000586438.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.48C>T
  hgvsp: ENST00000590800.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467323
  ensembl transcript: ENST00000590437
  gene symbol: ZBTB7C
  hgvsc: ENST00000590437.1:c.48C>T
  hgvsp: ENST00000590437.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.48C>T
  hgvsp: ENST00000586047.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000328732
  ensembl transcript: ENST00000332053
  gene symbol: ZBTB7C
  hgvsc: ENST00000332053.2:c.48C>T
  hgvsp: ENST00000332053.2:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.48C>T
  hgvsp: ENST00000590855.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.48C>T
  hgvsp: ENST00000592656.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.48C>T
  hgvsp: ENST00000588149.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.48C>T
  hgvsp: ENST00000586743.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.48C>T
  hgvsp: ENST00000589619.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.48C>T
  hgvsp: ENST00000592387.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.48C>T
  hgvsp: ENST00000587107.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.48C>T
  hgvsp: ENST00000591279.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.His16His
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

18-45567440-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567440
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567440
    reference: chr 18
allele count: 21
allele frequency: 1.769136156088356e-4
allele num: 118702
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.39C>T
  hgvsp: ENST00000591279.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.39C>T
  hgvsp: ENST00000588566.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.39C>T
  hgvsp: ENST00000593159.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.39C>T
  hgvsp: ENST00000588053.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.39C>T
  hgvsp: ENST00000590855.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.39C>T
  hgvsp: ENST00000586743.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.39C>T
  hgvsp: ENST00000588970.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.39C>T
  hgvsp: ENST00000588982.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467323
  ensembl transcript: ENST00000590437
  gene symbol: ZBTB7C
  hgvsc: ENST00000590437.1:c.39C>T
  hgvsp: ENST00000590437.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.39C>T
  hgvsp: ENST00000590178.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.39C>T
  hgvsp: ENST00000589194.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.39C>T
  hgvsp: ENST00000588149.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.39C>T
  hgvsp: ENST00000585404.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.39C>T
  hgvsp: ENST00000588028.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.39C>T
  hgvsp: ENST00000592656.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.39C>T
  hgvsp: ENST00000586047.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.39C>T
  hgvsp: ENST00000589170.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.39C>T
  hgvsp: ENST00000590800.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000439781
  ensembl transcript: ENST00000535628
  gene symbol: ZBTB7C
  hgvsc: ENST00000535628.2:c.39C>T
  hgvsp: ENST00000535628.2:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Phe13Phe
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP

18-45567449-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567449
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567449
    reference: chr 18
allele count: 1
allele frequency: 8.497043029025899e-6
allele num: 117688
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.30C>T
  hgvsp: ENST00000586438.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.30C>T
  hgvsp: ENST00000588982.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.30C>T
  hgvsp: ENST00000592656.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.30C>T
  hgvsp: ENST00000589194.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.30C>T
  hgvsp: ENST00000589619.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.30C>T
  hgvsp: ENST00000586047.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.30C>T
  hgvsp: ENST00000591526.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.30C>T
  hgvsp: ENST00000593159.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.30C>T
  hgvsp: ENST00000590855.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.30C>T
  hgvsp: ENST00000590374.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.30C>T
  hgvsp: ENST00000591279.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000439781
  ensembl transcript: ENST00000535628
  gene symbol: ZBTB7C
  hgvsc: ENST00000535628.2:c.30C>T
  hgvsp: ENST00000535628.2:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.30C>T
  hgvsp: ENST00000590800.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.30C>T
  hgvsp: ENST00000589170.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.30C>T
  hgvsp: ENST00000588566.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.30C>T
  hgvsp: ENST00000586525.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000328732
  ensembl transcript: ENST00000332053
  gene symbol: ZBTB7C
  hgvsc: ENST00000332053.2:c.30C>T
  hgvsp: ENST00000332053.2:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.30C>T
  hgvsp: ENST00000590178.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.30C>T
  hgvsp: ENST00000588053.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly10Gly
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

18-45567453-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567453
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567453
    reference: chr 18
allele count: 2
allele frequency: 1.704535769683127e-5
allele num: 117334
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.26T>C
  hgvsp: ENSP00000465832.1:p.Ile9Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.26T>C
  hgvsp: ENSP00000466006.1:p.Ile9Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.26T>C
  hgvsp: ENSP00000468782.1:p.Ile9Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.26T>C
  hgvsp: ENSP00000468502.1:p.Ile9Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.26T>C
  hgvsp: ENSP00000466944.1:p.Ile9Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.26T>C
  hgvsp: ENSP00000468152.1:p.Ile9Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.26T>C
  hgvsp: ENSP00000468752.1:p.Ile9Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.26T>C
  hgvsp: ENSP00000467758.1:p.Ile9Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.26T>C
  hgvsp: ENSP00000468537.1:p.Ile9Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.26T>C
  hgvsp: ENSP00000468814.1:p.Ile9Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.26T>C
  hgvsp: ENSP00000468019.1:p.Ile9Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467323
  ensembl transcript: ENST00000590437
  gene symbol: ZBTB7C
  hgvsc: ENST00000590437.1:c.26T>C
  hgvsp: ENSP00000467323.1:p.Ile9Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.26T>C
  hgvsp: ENSP00000468254.1:p.Ile9Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.26T>C
  hgvsp: ENSP00000468306.1:p.Ile9Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.26T>C
  hgvsp: ENSP00000465265.1:p.Ile9Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.26T>C
  hgvsp: ENSP00000468087.1:p.Ile9Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.26T>C
  hgvsp: ENSP00000466088.1:p.Ile9Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.26T>C
  hgvsp: ENSP00000467456.1:p.Ile9Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.26T>C
  hgvsp: ENSP00000467338.1:p.Ile9Thr
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile9Thr
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

18-45567465-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567465
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567465
    reference: chr 18
allele count: 29
allele frequency: 2.499482865614011e-4
allele num: 116024
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.14T>C
  hgvsp: ENSP00000467338.1:p.Ile5Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.14T>C
  hgvsp: ENSP00000465835.1:p.Ile5Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.14T>C
  hgvsp: ENSP00000468752.1:p.Ile5Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.14T>C
  hgvsp: ENSP00000468087.1:p.Ile5Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.14T>C
  hgvsp: ENSP00000465760.1:p.Ile5Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.14T>C
  hgvsp: ENSP00000468254.1:p.Ile5Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.14T>C
  hgvsp: ENSP00000466006.1:p.Ile5Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.14T>C
  hgvsp: ENSP00000468152.1:p.Ile5Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.14T>C
  hgvsp: ENSP00000465832.1:p.Ile5Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.14T>C
  hgvsp: ENSP00000468306.1:p.Ile5Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.14T>C
  hgvsp: ENSP00000467758.1:p.Ile5Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.14T>C
  hgvsp: ENSP00000467877.1:p.Ile5Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.14T>C
  hgvsp: ENSP00000468019.1:p.Ile5Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.14T>C
  hgvsp: ENSP00000465160.1:p.Ile5Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.14T>C
  hgvsp: ENSP00000468782.1:p.Ile5Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.14T>C
  hgvsp: ENSP00000465265.1:p.Ile5Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.14T>C
  hgvsp: ENSP00000468537.1:p.Ile5Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.14T>C
  hgvsp: ENSP00000465494.1:p.Ile5Thr
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.14T>C
  hgvsp: ENSP00000468502.1:p.Ile5Thr
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile5Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

18-45567470-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567470
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567470
    reference: chr 18
allele count: 2
allele frequency: 1.732441703336683e-5
allele num: 115444
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.9T>C
  hgvsp: ENST00000590374.1:c.9T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.9T>C
  hgvsp: ENST00000588566.1:c.9T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000439781
  ensembl transcript: ENST00000535628
  gene symbol: ZBTB7C
  hgvsc: ENST00000535628.2:c.9T>C
  hgvsp: ENST00000535628.2:c.9T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.9T>C
  hgvsp: ENST00000588053.1:c.9T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.9T>C
  hgvsp: ENST00000588028.1:c.9T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.9T>C
  hgvsp: ENST00000590800.1:c.9T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.9T>C
  hgvsp: ENST00000586047.1:c.9T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.9T>C
  hgvsp: ENST00000586438.1:c.9T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.9T>C
  hgvsp: ENST00000591526.1:c.9T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.9T>C
  hgvsp: ENST00000588982.1:c.9T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.9T>C
  hgvsp: ENST00000585404.1:c.9T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.9T>C
  hgvsp: ENST00000592387.1:c.9T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.9T>C
  hgvsp: ENST00000590855.1:c.9T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.9T>C
  hgvsp: ENST00000593159.1:c.9T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.9T>C
  hgvsp: ENST00000586525.1:c.9T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.9T>C
  hgvsp: ENST00000588970.1:c.9T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.9T>C
  hgvsp: ENST00000589619.1:c.9T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.9T>C
  hgvsp: ENST00000589077.1:c.9T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.9T>C
  hgvsp: ENST00000592656.1:c.9T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn3Asn
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

18-45567477-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567477
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567477
    reference: chr 18
allele count: 1
allele frequency: 8.741258741258741e-6
allele num: 114400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.2T>C
  hgvsp: ENSP00000468254.1:p.Met1?
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000328732
  ensembl transcript: ENST00000332053
  gene symbol: ZBTB7C
  hgvsc: ENST00000332053.2:c.2T>C
  hgvsp: ENSP00000328732.2:p.Met1?
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.2T>C
  hgvsp: ENSP00000468752.1:p.Met1?
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.2T>C
  hgvsp: ENSP00000465832.1:p.Met1?
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.2T>C
  hgvsp: ENSP00000465494.1:p.Met1?
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.2T>C
  hgvsp: ENSP00000466088.1:p.Met1?
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.2T>C
  hgvsp: ENSP00000465835.1:p.Met1?
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.2T>C
  hgvsp: ENSP00000467338.1:p.Met1?
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.2T>C
  hgvsp: ENSP00000468502.1:p.Met1?
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.2T>C
  hgvsp: ENSP00000467877.1:p.Met1?
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467323
  ensembl transcript: ENST00000590437
  gene symbol: ZBTB7C
  hgvsc: ENST00000590437.1:c.2T>C
  hgvsp: ENSP00000467323.1:p.Met1?
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.2T>C
  hgvsp: ENSP00000467758.1:p.Met1?
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.2T>C
  hgvsp: ENSP00000467456.1:p.Met1?
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000439781
  ensembl transcript: ENST00000535628
  gene symbol: ZBTB7C
  hgvsc: ENST00000535628.2:c.2T>C
  hgvsp: ENSP00000439781.1:p.Met1?
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: start_lost
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.2T>C
  hgvsp: ENSP00000468782.1:p.Met1?
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.2T>C
  hgvsp: ENSP00000465265.1:p.Met1?
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.2T>C
  hgvsp: ENSP00000467147.1:p.Met1?
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.2T>C
  hgvsp: ENSP00000468306.1:p.Met1?
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.2T>C
  hgvsp: ENSP00000466006.1:p.Met1?
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

18-45567483-TCAGC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567483
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567479
    reference: chr 18
allele count: 1
allele frequency: 8.811038468993955e-6
allele num: 113494
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-9_-6delGCTG
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-9_-6delGCTG
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-9_-6delGCTG
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-9_-6delGCTG
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-9_-6delGCTG
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-9_-6delGCTG
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-9_-6delGCTG
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-9_-6delGCTG
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-9_-6delGCTG
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-9_-6delGCTG
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-9_-6delGCTG
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000439781
  ensembl transcript: ENST00000535628
  gene symbol: ZBTB7C
  hgvsc: ENST00000535628.2:c.-9_-6delGCTG
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-9_-6delGCTG
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-9_-6delGCTG
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-9_-6delGCTG
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-9_-6delGCTG
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000328732
  ensembl transcript: ENST00000332053
  gene symbol: ZBTB7C
  hgvsc: ENST00000332053.2:c.-9_-6delGCTG
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-9_-6delGCTG
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-9_-6delGCTG
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-9_-6delGCTG
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-9_-6delGCTG
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: TCAGC
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/18-45567491-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567491
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567491
    reference: chr 18
allele count: 1
allele frequency: 8.947905295370353e-6
allele num: 111758
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-13T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-13T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-13T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-13T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-13T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-13T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-13T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-13T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-13T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-13T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-13T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-13T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-13T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-13T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-13T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-13T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000439781
  ensembl transcript: ENST00000535628
  gene symbol: ZBTB7C
  hgvsc: ENST00000535628.2:c.-13T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467323
  ensembl transcript: ENST00000590437
  gene symbol: ZBTB7C
  hgvsc: ENST00000590437.1:c.-13T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-13T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-13T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-13T>G
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

18-45567494-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567494
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567494
    reference: chr 18
allele count: 1
allele frequency: 8.980852821783957e-6
allele num: 111348
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-16G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000328732
  ensembl transcript: ENST00000332053
  gene symbol: ZBTB7C
  hgvsc: ENST00000332053.2:c.-16G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-16G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-16G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-16G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-16G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-16G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-16G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-16G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-16G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-16G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000439781
  ensembl transcript: ENST00000535628
  gene symbol: ZBTB7C
  hgvsc: ENST00000535628.2:c.-16G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-16G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-16G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-16G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-16G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-16G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-16G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-16G>C
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.-16G>C
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum

18-45567496-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567496
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567496
    reference: chr 18
allele count: 2
allele frequency: 1.799014140251142e-5
allele num: 111172
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-16-2A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-16-2A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-16-2A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-16-2A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-16-2A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-16-2A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-16-2A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-16-2A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-16-2A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-16-2A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-16-2A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-16-2A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000439781
  ensembl transcript: ENST00000535628
  gene symbol: ZBTB7C
  hgvsc: ENST00000535628.2:c.-16-2A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-16-2A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-16-2A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-16-2A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-16-2A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-16-2A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-16-2A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-16-2A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-16-2A>G
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.-16-2A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ

18-45567502-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567502
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567502
    reference: chr 18
allele count: 1
allele frequency: 9.098353198071149e-6
allele num: 109910
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.-16-8C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-16-8C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-16-8C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-16-8C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-16-8C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-16-8C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-16-8C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-16-8C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-16-8C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-16-8C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-16-8C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-16-8C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-16-8C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-16-8C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-16-8C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-16-8C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-16-8C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-16-8C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-16-8C>G
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.-16-8C>G
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

18-45567504-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567504
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567504
    reference: chr 18
allele count: 3
allele frequency: 2.731643356643357e-5
allele num: 109824
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-16-10G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-16-10G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-16-10G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-16-10G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-16-10G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-16-10G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-16-10G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-16-10G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-16-10G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-16-10G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-16-10G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-16-10G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-16-10G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-16-10G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-16-10G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-16-10G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-16-10G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-16-10G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-16-10G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-16-10G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000439781
  ensembl transcript: ENST00000535628
  gene symbol: ZBTB7C
  hgvsc: ENST00000535628.2:c.-16-10G>C
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/18-45567505-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567505
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567505
    reference: chr 18
allele count: 9
allele frequency: 8.202548258325587e-5
allele num: 109722
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-16-11T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000439781
  ensembl transcript: ENST00000535628
  gene symbol: ZBTB7C
  hgvsc: ENST00000535628.2:c.-16-11T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-16-11T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-16-11T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-16-11T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-16-11T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-16-11T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-16-11T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-16-11T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-16-11T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467323
  ensembl transcript: ENST00000590437
  gene symbol: ZBTB7C
  hgvsc: ENST00000590437.1:c.-16-11T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-16-11T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-16-11T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-16-11T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-16-11T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-16-11T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-16-11T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-16-11T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.-16-11T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-16-11T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-16-11T>G
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

18-45567508-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567508
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567508
    reference: chr 18
allele count: 5
allele frequency: 4.576323930513098e-5
allele num: 109258
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-16-14G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-16-14G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-16-14G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467323
  ensembl transcript: ENST00000590437
  gene symbol: ZBTB7C
  hgvsc: ENST00000590437.1:c.-16-14G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-16-14G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-16-14G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-16-14G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-16-14G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-16-14G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-16-14G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-16-14G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-16-14G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-16-14G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-16-14G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-16-14G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-16-14G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-16-14G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-16-14G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-16-14G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-16-14G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-16-14G>A
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

18-45567510-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567510
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567510
    reference: chr 18
allele count: 1
allele frequency: 9.170778232240788e-6
allele num: 109042
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467323
  ensembl transcript: ENST00000590437
  gene symbol: ZBTB7C
  hgvsc: ENST00000590437.1:c.-16-16C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-16-16C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000439781
  ensembl transcript: ENST00000535628
  gene symbol: ZBTB7C
  hgvsc: ENST00000535628.2:c.-16-16C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.-16-16C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-16-16C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-16-16C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-16-16C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-16-16C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-16-16C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-16-16C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-16-16C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-16-16C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-16-16C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-16-16C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-16-16C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-16-16C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-16-16C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-16-16C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-16-16C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-16-16C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-16-16C>G
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

18-45567510-GAGA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567510
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567507
    reference: chr 18
allele count: 1
allele frequency: 9.170778232240788e-6
allele num: 109042
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-16-19_-16-17delTCT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-16-19_-16-17delTCT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-16-19_-16-17delTCT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-16-19_-16-17delTCT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-16-19_-16-17delTCT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-16-19_-16-17delTCT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-16-19_-16-17delTCT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-16-19_-16-17delTCT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000439781
  ensembl transcript: ENST00000535628
  gene symbol: ZBTB7C
  hgvsc: ENST00000535628.2:c.-16-19_-16-17delTCT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-16-19_-16-17delTCT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-16-19_-16-17delTCT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.-16-19_-16-17delTCT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-16-19_-16-17delTCT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-16-19_-16-17delTCT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-16-19_-16-17delTCT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-16-19_-16-17delTCT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-16-19_-16-17delTCT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-16-19_-16-17delTCT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-16-19_-16-17delTCT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-16-19_-16-17delTCT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-16-19_-16-17delTCT
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: GAGA
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

18-45567512-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567512
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567512
    reference: chr 18
allele count: 1
allele frequency: 9.201324990798676e-6
allele num: 108680
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-16-18C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-16-18C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-16-18C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-16-18C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-16-18C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-16-18C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-16-18C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-16-18C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-16-18C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-16-18C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-16-18C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-16-18C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-16-18C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-16-18C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-16-18C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-16-18C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000439781
  ensembl transcript: ENST00000535628
  gene symbol: ZBTB7C
  hgvsc: ENST00000535628.2:c.-16-18C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-16-18C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.-16-18C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-16-18C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-16-18C>T
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

18-45567516-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567516
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567516
    reference: chr 18
allele count: 2
allele frequency: 1.846449278038332e-5
allele num: 108316
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-16-22T>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-16-22T>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-16-22T>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-16-22T>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-16-22T>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-16-22T>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-16-22T>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-16-22T>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-16-22T>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.-16-22T>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-16-22T>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-16-22T>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-16-22T>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-16-22T>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-16-22T>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-16-22T>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-16-22T>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-16-22T>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-16-22T>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-16-22T>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-16-22T>C
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/18-45567517-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567517
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567517
    reference: chr 18
allele count: 1
allele frequency: 9.263547938860584e-6
allele num: 107950
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-16-23T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-16-23T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-16-23T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.-16-23T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-16-23T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-16-23T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-16-23T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-16-23T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-16-23T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-16-23T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-16-23T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-16-23T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-16-23T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-16-23T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-16-23T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-16-23T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000439781
  ensembl transcript: ENST00000535628
  gene symbol: ZBTB7C
  hgvsc: ENST00000535628.2:c.-16-23T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-16-23T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-16-23T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-16-23T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-16-23T>G
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

18-45567531-AGCGT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567531
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567527
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 105270
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-16-41_-16-38delACGC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-16-41_-16-38delACGC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-16-41_-16-38delACGC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-16-41_-16-38delACGC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-16-41_-16-38delACGC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-16-41_-16-38delACGC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-16-41_-16-38delACGC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-16-41_-16-38delACGC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-16-41_-16-38delACGC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-16-41_-16-38delACGC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-16-41_-16-38delACGC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-16-41_-16-38delACGC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-16-41_-16-38delACGC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-16-41_-16-38delACGC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-16-41_-16-38delACGC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-16-41_-16-38delACGC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-16-41_-16-38delACGC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-16-41_-16-38delACGC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-16-41_-16-38delACGC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467323
  ensembl transcript: ENST00000590437
  gene symbol: ZBTB7C
  hgvsc: ENST00000590437.1:c.-16-41_-16-38delACGC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000439781
  ensembl transcript: ENST00000535628
  gene symbol: ZBTB7C
  hgvsc: ENST00000535628.2:c.-16-41_-16-38delACGC
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: AGCGT
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

18-45567534-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567534
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567534
    reference: chr 18
allele count: 1
allele frequency: 9.698568491290685e-6
allele num: 103108
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000439781
  ensembl transcript: ENST00000535628
  gene symbol: ZBTB7C
  hgvsc: ENST00000535628.2:c.-16-40C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-16-40C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-16-40C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467323
  ensembl transcript: ENST00000590437
  gene symbol: ZBTB7C
  hgvsc: ENST00000590437.1:c.-16-40C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-16-40C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-16-40C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-16-40C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-16-40C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-16-40C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-16-40C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-16-40C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-16-40C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-16-40C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-16-40C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-16-40C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-16-40C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-16-40C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-16-40C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-16-40C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-16-40C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-16-40C>T
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

18-45567535-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567535
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567534
    reference: chr 18
allele count: 2
allele frequency: 1.938397720444281e-5
allele num: 103178
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-16-42delC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-16-42delC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-16-42delC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-16-42delC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-16-42delC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-16-42delC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-16-42delC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-16-42delC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.-16-42delC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-16-42delC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-16-42delC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-16-42delC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467323
  ensembl transcript: ENST00000590437
  gene symbol: ZBTB7C
  hgvsc: ENST00000590437.1:c.-16-42delC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-16-42delC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000439781
  ensembl transcript: ENST00000535628
  gene symbol: ZBTB7C
  hgvsc: ENST00000535628.2:c.-16-42delC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-16-42delC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-16-42delC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-16-42delC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-16-42delC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-16-42delC
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-16-42delC
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: TG
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum

18-45567537-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567537
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567537
    reference: chr 18
allele count: 1
allele frequency: 9.886698435924308e-6
allele num: 101146
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-16-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-16-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000439781
  ensembl transcript: ENST00000535628
  gene symbol: ZBTB7C
  hgvsc: ENST00000535628.2:c.-16-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-16-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-16-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-16-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-16-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-16-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-16-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-16-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-16-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-16-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-16-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-16-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-16-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-16-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-16-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.-16-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-16-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-16-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-16-43C>T
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum

18-45567540-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45567540
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45567540
    reference: chr 18
allele count: 1
allele frequency: 1.00965227575623e-5
allele num: 99044
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-16-46G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-16-46G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-16-46G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000439781
  ensembl transcript: ENST00000535628
  gene symbol: ZBTB7C
  hgvsc: ENST00000535628.2:c.-16-46G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-16-46G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-16-46G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-16-46G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-16-46G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-16-46G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-16-46G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-16-46G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-16-46G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-16-46G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-16-46G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-16-46G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-16-46G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-16-46G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-16-46G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-16-46G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-16-46G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467323
  ensembl transcript: ENST00000590437
  gene symbol: ZBTB7C
  hgvsc: ENST00000590437.1:c.-16-46G>C
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

18-45688785-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45688785
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45688785
    reference: chr 18
allele count: 1
allele frequency: 8.130081300813008e-5
allele num: 12300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-17+2717C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-66-17C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-17+23520C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-66-17C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-66-17C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-85+2717C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-17+2717C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-17+22910C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-17+17973C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-17+23520C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-17+23520C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-66-17C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-17+23520C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-85+2713C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-66-17C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-17+17916C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.-17+2717C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-246+23520C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-17+2717C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-17+23520C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-168+23520C>T
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

18-45688803-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45688803
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45688804
    reference: chr 18
allele count: 5
allele frequency: 4.077638231936063e-4
allele num: 12262
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-17+2698dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-17+22891dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-66-36dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-66-36dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-17+2698dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-17+23501dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467323
  ensembl transcript: ENST00000590437
  gene symbol: ZBTB7C
  hgvsc: ENST00000590437.1:c.-146+2698dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-146+23501dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-17+23501dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-246+23501dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-17+2698dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-85+2698dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-17+17897dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-17+17954dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-17+23501dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-17+2698dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-66-36dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-66-36dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-66-36dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-17+2698dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.-17+2698dupA
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

18-45691461-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45691461
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45691461
    reference: chr 18
allele count: 1
allele frequency: 9.800078400627205e-5
allele num: 10204
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-17+20844G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-17+41G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-17+20844G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-17+15297G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-17+41G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-67+41G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-17+20844G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-67+41G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-17+41G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-67+41G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467323
  ensembl transcript: ENST00000590437
  gene symbol: ZBTB7C
  hgvsc: ENST00000590437.1:c.-146+41G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-246+20844G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-67+41G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-17+20844G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-85+37G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-67+41G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-85+41G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-17+41G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-17+20234G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-146+20844G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-85+41G>A
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

18-45691531-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45691531
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45691531
    reference: chr 18
allele count: 9
allele frequency: 7.333767926988266e-4
allele num: 12272
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-118A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-46A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-96A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-46A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-46A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-246+20774A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-114A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.-46A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-17+20774A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-17+20774A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-146+20774A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467323
  ensembl transcript: ENST00000590437
  gene symbol: ZBTB7C
  hgvsc: ENST00000590437.1:c.-175A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-46A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-114A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-17+20774A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-17+15170A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-96A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-17+15227A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-46A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-17+20774A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-96A>G
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 1
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

18-45691551-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45691551
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45691551
    reference: chr 18
allele count: 1
allele frequency: 8.135372600065082e-5
allele num: 12292
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-66C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-246+20754C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-66C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-134C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-116C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-116C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-116C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-116C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-116C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-17+20754C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-66C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-66C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467323
  ensembl transcript: ENST00000590437
  gene symbol: ZBTB7C
  hgvsc: ENST00000590437.1:c.-195C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-17+20754C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-138C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-66C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.-66C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-17+15207C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-17+15150C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-17+20144C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-168+20754C>T
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

18-45691554-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45691554
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45691554
    reference: chr 18
allele count: 1
allele frequency: 8.132726089785297e-5
allele num: 12296
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-168+20751G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.-69G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-69G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467323
  ensembl transcript: ENST00000590437
  gene symbol: ZBTB7C
  hgvsc: ENST00000590437.1:c.-198G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-69G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-17+15147G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-69G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-69G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-137G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-119G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-17+20751G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-17+20141G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-246+20751G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-141G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-146+20751G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-137G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-17+20751G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-17+20751G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-119G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-119G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-17+20751G>C
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

18-45691590-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45691590
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45691590
    reference: chr 18
allele count: 1
allele frequency: 8.143322475570033e-5
allele num: 12280
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-105G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-105G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-155G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-173G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-173G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-105G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-155G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-168+20715G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-177G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-17+20715G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-105G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-17+20715G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-17+20105G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-17+20715G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467323
  ensembl transcript: ENST00000590437
  gene symbol: ZBTB7C
  hgvsc: ENST00000590437.1:c.-234G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-17+15111G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-155G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-105G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-155G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-17+20715G>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-17+20715G>C
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

18-45691598-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45691598
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45691598
    reference: chr 18
allele count: 15
allele frequency: 1.223491027732463e-3
allele num: 12260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-113G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-113G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-113G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-181G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-17+15103G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-185G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-163G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-163G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-163G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.-113G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-163G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-181G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467323
  ensembl transcript: ENST00000590437
  gene symbol: ZBTB7C
  hgvsc: ENST00000590437.1:c.-242G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-246+20707G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-113G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-17+20097G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-113G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-17+20707G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-163G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-113G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-17+20707G>A
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

18-45691668-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45691668
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45691668
    reference: chr 18
allele count: 5
allele frequency: 4.615100609193281e-4
allele num: 10834
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-233A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-146+20637A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-139-44A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.-183A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467323
  ensembl transcript: ENST00000590437
  gene symbol: ZBTB7C
  hgvsc: ENST00000590437.1:c.-312A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-17+20637A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-143-40A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-17+20637A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-143-40A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-211-40A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-189-44A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-193-40A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-17+20637A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-17+15033A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-168+20637A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-143-40A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-193-40A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-143-40A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-17+20637A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-215-40A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-17+15090A>G
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum

18-45691671-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45691671
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45691671
    reference: chr 18
allele count: 1
allele frequency: 9.366804046459348e-5
allele num: 10676
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-211-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-168+20634C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-143-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-193-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468782
  ensembl transcript: ENST00000588982
  gene symbol: ZBTB7C
  hgvsc: ENST00000588982.1:c.-236C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-215-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-17+15030C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-193-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-143-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-139-47C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-17+20634C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-17+20634C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-146+20634C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-143-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-17+20634C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467323
  ensembl transcript: ENST00000590437
  gene symbol: ZBTB7C
  hgvsc: ENST00000590437.1:c.-315C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-143-43C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-189-47C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468254
  ensembl transcript: ENST00000586438
  gene symbol: ZBTB7C
  hgvsc: ENST00000586438.1:c.-186C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-207-47C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-143-43C>T
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/18-45706656-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45706656
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45706656
    reference: chr 18
allele count: 22
allele frequency: 1.785134696527102e-3
allele num: 12324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-17+102G>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-17+5649G>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-17+5649G>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-194+5649G>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-17+5039G>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-216+5649G>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-212+5649G>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-144+5649G>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-144+5039G>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-17+5649G>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-144+5649G>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-190+5649G>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-194+5039G>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-140+5039G>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-17+5649G>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-17+5649G>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-168+5649G>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-144+5649G>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-246+5649G>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-194+5649G>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-144+5649G>T
  variant of: http://identifiers.org/hgnc/31700
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 1
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

18-45706671-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45706671
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45706671
    reference: chr 18
allele count: 1
allele frequency: 8.132726089785297e-5
allele num: 12296
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-168+5634A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-144+5634A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-208+5634A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-190+5634A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-17+87A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-144+5634A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-17+5634A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-17+5634A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-17+5024A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-194+5024A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-17+5634A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-246+5634A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-140+5024A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-17+5634A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-146+5634A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-144+5634A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-194+5634A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-216+5634A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-144+5634A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-144+5024A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-17+5634A>C
  variant of: http://identifiers.org/hgnc/31700
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

18-45706700-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45706700
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45706700
    reference: chr 18
allele count: 21
allele frequency: 1.708428246013667e-3
allele num: 12292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-17+58G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-140+4995G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-216+5605G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-17+5605G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-144+5605G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-246+5605G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-17+5605G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-194+5605G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-17+5605G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-144+5605G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-17+1G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-17+5605G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-168+5605G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-194+4995G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-194+5605G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-144+5605G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-17+4995G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-144+4995G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-144+5605G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-190+5605G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-17+5605G>A
  variant of: http://identifiers.org/hgnc/31700
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.-17+1G>A
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

18-45706710-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45706710
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45706710
    reference: chr 18
allele count: 1
allele frequency: 8.139345596614032e-5
allele num: 12286
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-144+5595A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-246+5595A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-17+5595A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-208+5595A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-144+4985A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-17+5595A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-216+5595A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-17+5595A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-144+5595A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-144+5595A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-17+48A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-17+5595A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-168+5595A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-26A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-194+4985A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-17+5595A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-140+4985A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-194+5595A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-194+5595A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-144+5595A>C
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-17+4985A>C
  variant of: http://identifiers.org/hgnc/31700
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD

18-45706735-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45706735
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45706735
    reference: chr 18
allele count: 1
allele frequency: 8.152616990053807e-5
allele num: 12266
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-216+5570A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-17+5570A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-194+4960A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-144+4960A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-17+5570A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-194+5570A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-246+5570A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-17+23A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-208+5570A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-144+5570A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-51A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-144+5570A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-144+5570A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-17+5570A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-17+5570A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-190+5570A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-194+5570A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-17+4960A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-17+5570A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-168+5570A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-140+4960A>G
  variant of: http://identifiers.org/hgnc/31700
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

18-45706749-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45706749
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45706749
    reference: chr 18
allele count: 1
allele frequency: 8.171269815329302e-5
allele num: 12238
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-144+5556C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-144+4946C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-246+5556C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-17+9C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-140+4946C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-212+5556C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-144+5556C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-144+5556C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-17+5556C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-216+5556C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-168+5556C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-65C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-144+5556C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-190+5556C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-194+4946C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-17+5556C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-17+5556C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-208+5556C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-146+5556C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-17+5556C>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-17+5556C>G
  variant of: http://identifiers.org/hgnc/31700
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

18-45711660-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45711660
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45711660
    reference: chr 18
allele count: 1
allele frequency: 1.136621959536258e-4
allele num: 8798
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-194+35C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-140+35C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-212+645C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-144+645C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-108+645C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-146+645C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-17+645C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-190+645C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-216+645C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-17+645C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-17+645C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-144+645C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-17+35C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-17+645C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-208+645C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-144+645C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-144+35C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-17+645C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-168+645C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-246+645C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-194+645C>T
  variant of: http://identifiers.org/hgnc/31700
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

18-45711664-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45711664
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45711664
    reference: chr 18
allele count: 1
allele frequency: 1.113089937666963e-4
allele num: 8984
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-144+641C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-208+641C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-212+641C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-17+641C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-144+31C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-144+641C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-194+31C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-190+641C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-168+641C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-17+641C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-216+641C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-17+641C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-17+641C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-194+641C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-17+641C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-146+641C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-140+31C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-144+641C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-108+641C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-17+31C>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-246+641C>T
  variant of: http://identifiers.org/hgnc/31700
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/18-45711717-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45711717
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45711718
    reference: chr 18
allele count: 1
allele frequency: 1.003009027081244e-4
allele num: 9970
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-144+587dupT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-144+587dupT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-246+587dupT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-208+587dupT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-163dupT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-217dupT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-216+587dupT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-167dupT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-188dupT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-17+587dupT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-17+587dupT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-190+587dupT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-108+587dupT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-194+587dupT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-144+587dupT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-40dupT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-17+587dupT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-17+587dupT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-168+587dupT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-144+587dupT
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-17+587dupT
  variant of: http://identifiers.org/hgnc/31700
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

18-45711734-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45711734
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45711734
    reference: chr 18
allele count: 1
allele frequency: 1.023751023751024e-4
allele num: 9768
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-179A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-208+571A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-17+571A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-216+571A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-246+571A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-17+571A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-233A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-144+571A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-194+571A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-108+571A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-146+571A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-168+571A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-194+571A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-212+571A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-17+571A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-204A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-144+571A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-144+571A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-56A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-190+571A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-17+571A>G
  variant of: http://identifiers.org/hgnc/31700
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

18-45711737-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45711737
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45711737
    reference: chr 18
allele count: 1
allele frequency: 1.030715316429602e-4
allele num: 9702
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-168+568A>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-246+568A>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-17+568A>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-144+568A>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-144+568A>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-212+568A>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-108+568A>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-236A>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-146+568A>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-59A>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-207A>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-182A>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-194+568A>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-144+568A>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-17+568A>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-190+568A>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-186A>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-216+568A>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-17+568A>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-208+568A>T
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-144+568A>T
  variant of: http://identifiers.org/hgnc/31700
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

18-45711740-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45711740
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45711740
    reference: chr 18
allele count: 2858
allele frequency: 2.906243644498678e-1
allele num: 9834
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-194+565A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-168+565A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-212+565A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-208+565A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-190+565A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-17+565A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-185A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-194+565A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-210A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-17+565A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-62A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-144+565A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466944
  ensembl transcript: ENST00000586047
  gene symbol: ZBTB7C
  hgvsc: ENST00000586047.1:c.-17+565A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-108+565A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-239A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-216+565A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-144+565A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-144+565A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-144+565A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-189A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-17+565A>G
  variant of: http://identifiers.org/hgnc/31700
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 427
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

18-45778622-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45778622
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45778622
    reference: chr 18
allele count: 1
allele frequency: 2.5e-1
allele num: 4
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-296A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-358-66256A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-387-66256A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-205-66256A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-169-66256A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-277-66256A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-229-66256A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-251-66256A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-205-66256A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-333-66256A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-78-66256A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-255-66256A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-78-66256A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-205-66256A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-269-66256A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-207-66256A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-255-66256A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-78-66256A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-78-66256A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-210-66256A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-337-66256A>G
  variant of: http://identifiers.org/hgnc/31700
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

18-45778702-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45778702
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45778703
    reference: chr 18
allele count: 0
allele frequency: NaN
allele num: 0
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-205-66337dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-343-34dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-169-66337dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-78-66337dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000268960
  ensembl protein: ENSP00000471539
  ensembl transcript: ENST00000600091
  gene symbol: AC091150.1
  hgvsc: ENST00000600091.1:c.32dupT
  hgvsp: ENSP00000471539.1:p.Ser12GlufsTer10
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-387-66337dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-210-66337dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-358-66337dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-251-66337dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-78-66337dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-269-66337dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-333-66337dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-205-66337dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-78-66337dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-307-66337dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-78-66337dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-255-66337dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-229-66337dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-255-66337dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-207-66337dupA
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-277-66337dupA
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: frameshift
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser12GlufsTer10
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

18-45779009-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45779009
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45779009
    reference: chr 18
allele count: 3
allele frequency: 1.0e-1
allele num: 30
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-78-66643A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-333-66643A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-277-66643A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-251-66643A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-205-66643A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-210-66643A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-343-340A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000268960
  ensembl protein: ENSP00000471539
  ensembl transcript: ENST00000600091
  gene symbol: AC091150.1
  hgvsc: ENST00000600091.1:c.338T>C
  hgvsp: ENSP00000471539.1:p.Met113Thr
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-169-66643A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-78-66643A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-205-66643A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-207-66643A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-358-66643A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-78-66643A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-269-66643A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-255-66643A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-78-66643A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-387-66643A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-229-66643A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-307-66643A>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-273-66643A>G
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Met113Thr
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

18-45779022-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45779022
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45779022
    reference: chr 18
allele count: 3
allele frequency: 7.5e-2
allele num: 40
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-78-66656G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-207-66656G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-387-66656G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-277-66656G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-78-66656G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-205-66656G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-169-66656G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-343-353G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000268960
  ensembl protein: ENSP00000471539
  ensembl transcript: ENST00000600091
  gene symbol: AC091150.1
  hgvsc: ENST00000600091.1:c.351C>T
  hgvsp: ENST00000600091.1:c.351C>T(p.%3D)
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-307-66656G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-251-66656G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-210-66656G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-273-66656G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-333-66656G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-78-66656G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465832
  ensembl transcript: ENST00000593159
  gene symbol: ZBTB7C
  hgvsc: ENST00000593159.1:c.-269-66656G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-255-66656G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466088
  ensembl transcript: ENST00000588053
  gene symbol: ZBTB7C
  hgvsc: ENST00000588053.1:c.-255-66656G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-78-66656G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-337-66656G>A
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468537
  ensembl transcript: ENST00000586525
  gene symbol: ZBTB7C
  hgvsc: ENST00000586525.1:c.-205-66656G>A
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu117Leu
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/18-45779072-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45779072
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 45779072
    reference: chr 18
allele count: 5
allele frequency: 8.928571428571429e-2
allele num: 56
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468752
  ensembl transcript: ENST00000591526
  gene symbol: ZBTB7C
  hgvsc: ENST00000591526.1:c.-251-66706T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467338
  ensembl transcript: ENST00000589170
  gene symbol: ZBTB7C
  hgvsc: ENST00000589170.1:c.-343-403T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468659
  ensembl transcript: ENST00000589619
  gene symbol: ZBTB7C
  hgvsc: ENST00000589619.1:c.-277-66706T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465760
  ensembl transcript: ENST00000587107
  gene symbol: ZBTB7C
  hgvsc: ENST00000587107.1:c.-337-66706T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000466006
  ensembl transcript: ENST00000586743
  gene symbol: ZBTB7C
  hgvsc: ENST00000586743.1:c.-273-66706T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000268960
  ensembl protein: ENSP00000471539
  ensembl transcript: ENST00000600091
  gene symbol: AC091150.1
  hgvsc: ENST00000600091.1:c.401A>C
  hgvsp: ENSP00000471539.1:p.Glu134Ala
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468814
  ensembl transcript: ENST00000588149
  gene symbol: ZBTB7C
  hgvsc: ENST00000588149.1:c.-210-66706T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467147
  ensembl transcript: ENST00000589077
  gene symbol: ZBTB7C
  hgvsc: ENST00000589077.1:c.-169-66706T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467877
  ensembl transcript: ENST00000590800
  gene symbol: ZBTB7C
  hgvsc: ENST00000590800.1:c.-78-66706T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468087
  ensembl transcript: ENST00000592656
  gene symbol: ZBTB7C
  hgvsc: ENST00000592656.1:c.-387-66706T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468502
  ensembl transcript: ENST00000588970
  gene symbol: ZBTB7C
  hgvsc: ENST00000588970.1:c.-229-66706T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000464724
  ensembl transcript: ENST00000585404
  gene symbol: ZBTB7C
  hgvsc: ENST00000585404.1:c.-307-66706T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468019
  ensembl transcript: ENST00000589194
  gene symbol: ZBTB7C
  hgvsc: ENST00000589194.1:c.-358-66706T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465265
  ensembl transcript: ENST00000591279
  gene symbol: ZBTB7C
  hgvsc: ENST00000591279.1:c.-78-66706T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468306
  ensembl transcript: ENST00000590855
  gene symbol: ZBTB7C
  hgvsc: ENST00000590855.1:c.-205-66706T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465494
  ensembl transcript: ENST00000590374
  gene symbol: ZBTB7C
  hgvsc: ENST00000590374.1:c.-333-66706T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465835
  ensembl transcript: ENST00000592387
  gene symbol: ZBTB7C
  hgvsc: ENST00000592387.1:c.-255-66706T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467456
  ensembl transcript: ENST00000588566
  gene symbol: ZBTB7C
  hgvsc: ENST00000588566.1:c.-78-66706T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000467758
  ensembl transcript: ENST00000591405
  gene symbol: ZBTB7C
  hgvsc: ENST00000591405.1:c.-78-66706T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000468152
  ensembl transcript: ENST00000588028
  gene symbol: ZBTB7C
  hgvsc: ENST00000588028.1:c.-207-66706T>G
  variant of: http://identifiers.org/hgnc/31700
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184828
  ensembl protein: ENSP00000465160
  ensembl transcript: ENST00000590178
  gene symbol: ZBTB7C
  hgvsc: ENST00000590178.1:c.-205-66706T>G
  variant of: http://identifiers.org/hgnc/31700
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu134Ala
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/18-46145905-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46145905
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 46145905
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 15968
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134030
  ensembl protein: ENSP00000372459
  ensembl transcript: ENST00000382998
  gene symbol: CTIF
  hgvsc: ENST00000382998.4:c.-28-4C>A
  variant of: http://identifiers.org/hgnc/23925
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134030
  ensembl protein: ENSP00000465405
  ensembl transcript: ENST00000587752
  gene symbol: CTIF
  hgvsc: ENST00000587752.1:c.-28-4C>A
  variant of: http://identifiers.org/hgnc/23925
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134030
  ensembl protein: ENSP00000467965
  ensembl transcript: ENST00000591412
  gene symbol: CTIF
  hgvsc: ENST00000591412.1:c.-28-4C>A
  variant of: http://identifiers.org/hgnc/23925
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134030
  ensembl protein: ENSP00000467957
  ensembl transcript: ENST00000588345
  gene symbol: CTIF
  hgvsc: ENST00000588345.1:c.-28-4C>A
  variant of: http://identifiers.org/hgnc/23925
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134030
  ensembl protein: ENSP00000467425
  ensembl transcript: ENST00000591387
  gene symbol: CTIF
  hgvsc: ENST00000591387.1:c.-28-4C>A
  variant of: http://identifiers.org/hgnc/23925
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000134030
  ensembl protein: ENSP00000256413
  ensembl transcript: ENST00000256413
  gene symbol: CTIF
  hgvsc: ENST00000256413.3:c.-28-4C>A
  variant of: http://identifiers.org/hgnc/23925
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20469
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31203
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5533
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24542
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 792
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1369
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2318
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1124
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4366
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2130
  bin: 3.25e1
  variant carriers: 0
hgvs: c.-28-4C>A
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

18-46145912-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 46145912
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 46145912
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 17444
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000134030
  ensembl protein: ENSP00000467425
  ensembl transcript: ENST00000591387
  gene symbol: CTIF
  hgvsc: ENST00000591387.1:c.-25C>T
  variant of: http://identifiers.org/hgnc/23925
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000134030
  ensembl protein: ENSP00000465405
  ensembl transcript: ENST00000587752
  gene symbol: CTIF
  hgvsc: ENST00000587752.1:c.-25C>T
  variant of: http://identifiers.org/hgnc/23925
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000134030
  ensembl protein: ENSP00000372459
  ensembl transcript: ENST00000382998
  gene symbol: CTIF
  hgvsc: ENST00000382998.4:c.-25C>T
  variant of: http://identifiers.org/hgnc/23925
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000134030
  ensembl protein: ENSP00000467957
  ensembl transcript: ENST00000588345
  gene symbol: CTIF
  hgvsc: ENST00000588345.1:c.-25C>T
  variant of: http://identifiers.org/hgnc/23925
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000134030
  ensembl protein: ENSP00000256413
  ensembl transcript: ENST00000256413
  gene symbol: CTIF
  hgvsc: ENST00000256413.3:c.-25C>T
  variant of: http://identifiers.org/hgnc/23925
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000134030
  ensembl protein: ENSP00000467965
  ensembl transcript: ENST00000591412
  gene symbol: CTIF
  hgvsc: ENST00000591412.1:c.-25C>T
  variant of: http://identifiers.org/hgnc/23925
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 5855
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16066
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 455
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 285
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 255
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1977
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28931
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9611
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17919
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 708
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1547
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 57
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1839
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46374
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7758
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10310
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504347564461293e-5
allele num: 66474
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.734e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.509e0

FS
type: SiteQuality
SIO_000300: 3.526e0

QD
type: SiteQuality
SIO_000300: 4.64e0

VQSLOD
type: SiteQuality
SIO_000300: -2.093e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e0

MQRankSum
type: SiteQuality
SIO_000300: 4.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.305e0

DP
type: SiteQuality
SIO_000300: 1.623291e6

GenotypeDepth
all individuals: 1969
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 708
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 523
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 17805
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 323
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 623
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 256
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28703
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7643
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46052
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 899
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 264
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 778
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1826
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1528
bin: 7.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157943492357573e-4
allele num: 8636
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16024
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e0

QD
type: SiteQuality
SIO_000300: 1.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.97e-1

FS
type: SiteQuality
SIO_000300: 8.4997e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

MQ
type: SiteQuality
SIO_000300: 5.966e1

VQSLOD
type: SiteQuality
SIO_000300: -6.564e0

DP
type: SiteQuality
SIO_000300: 1.616921e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.84e0

MQRankSum
type: SiteQuality
SIO_000300: 1.34e0

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466088
ensembl transcript: ENST00000588053
gene symbol: ZBTB7C
hgvsc: ENST00000588053.1:c.54T>C
hgvsp: ENST00000588053.1:c.54T>C(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467323
ensembl transcript: ENST00000590437
gene symbol: ZBTB7C
hgvsc: ENST00000590437.1:c.54T>C
hgvsp: ENST00000590437.1:c.54T>C(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000328732
ensembl transcript: ENST00000332053
gene symbol: ZBTB7C
hgvsc: ENST00000332053.2:c.54T>C
hgvsp: ENST00000332053.2:c.54T>C(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467877
ensembl transcript: ENST00000590800
gene symbol: ZBTB7C
hgvsc: ENST00000590800.1:c.54T>C
hgvsp: ENST00000590800.1:c.54T>C(p.%3D)
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 9524
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 611
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17747
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28606
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 708
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1965
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 342
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 707
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 255
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1053
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 183
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 7635
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1526
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 777
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45890
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1821
bin: 7.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66288
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157943492357573e-4
allele num: 8636
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.04e-1

FS
type: SiteQuality
SIO_000300: 4.404e0

MQRankSum
type: SiteQuality
SIO_000300: 7.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.84e-1

QD
type: SiteQuality
SIO_000300: 1.163e1

DP
type: SiteQuality
SIO_000300: 1.613691e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.6e-2

MQ
type: SiteQuality
SIO_000300: 5.952e1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000464724
ensembl transcript: ENST00000585404
gene symbol: ZBTB7C
hgvsc: ENST00000585404.1:c.48C>T
hgvsp: ENST00000585404.1:c.48C>T(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468537
ensembl transcript: ENST00000586525
gene symbol: ZBTB7C
hgvsc: ENST00000586525.1:c.48C>T
hgvsp: ENST00000586525.1:c.48C>T(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465160
ensembl transcript: ENST00000590178
gene symbol: ZBTB7C
hgvsc: ENST00000590178.1:c.48C>T
hgvsp: ENST00000590178.1:c.48C>T(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466088
ensembl transcript: ENST00000588053
gene symbol: ZBTB7C
hgvsc: ENST00000588053.1:c.48C>T
hgvsp: ENST00000588053.1:c.48C>T(p.%3D)
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 255
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28298
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1959
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 837
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9442
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17575
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 711
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 956
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 413
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 27
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 7.25e1
variant carriers: 2

GenotypeDepth
all individuals: 5
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 46
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1805
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 281
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7558
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 774
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1452
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45375
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1516
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 97
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15554
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 10
allele frequency: 8.667013347200555e-4
allele num: 11538
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66172
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.968e1

FS
type: SiteQuality
SIO_000300: 1.094e0

QD
type: SiteQuality
SIO_000300: 1.275e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.605584e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.931e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-2

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465494
ensembl transcript: ENST00000590374
gene symbol: ZBTB7C
hgvsc: ENST00000590374.1:c.39C>T
hgvsp: ENST00000590374.1:c.39C>T(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468752
ensembl transcript: ENST00000591526
gene symbol: ZBTB7C
hgvsc: ENST00000591526.1:c.39C>T
hgvsp: ENST00000591526.1:c.39C>T(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468254
ensembl transcript: ENST00000586438
gene symbol: ZBTB7C
hgvsc: ENST00000586438.1:c.39C>T
hgvsp: ENST00000586438.1:c.39C>T(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465835
ensembl transcript: ENST00000592387
gene symbol: ZBTB7C
hgvsc: ENST00000592387.1:c.39C>T
hgvsp: ENST00000592387.1:c.39C>T(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468537
ensembl transcript: ENST00000586525
gene symbol: ZBTB7C
hgvsc: ENST00000586525.1:c.39C>T
hgvsp: ENST00000586525.1:c.39C>T(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467758
ensembl transcript: ENST00000591405
gene symbol: ZBTB7C
hgvsc: ENST00000591405.1:c.39C>T
hgvsp: ENST00000591405.1:c.39C>T(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465760
ensembl transcript: ENST00000587107
gene symbol: ZBTB7C
hgvsc: ENST00000587107.1:c.39C>T
hgvsp: ENST00000587107.1:c.39C>T(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000328732
ensembl transcript: ENST00000332053
gene symbol: ZBTB7C
hgvsc: ENST00000332053.2:c.39C>T
hgvsp: ENST00000332053.2:c.39C>T(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467147
ensembl transcript: ENST00000589077
gene symbol: ZBTB7C
hgvsc: ENST00000589077.1:c.39C>T
hgvsp: ENST00000589077.1:c.39C>T(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468659
ensembl transcript: ENST00000589619
gene symbol: ZBTB7C
hgvsc: ENST00000589619.1:c.39C>T
hgvsp: ENST00000589619.1:c.39C>T(p.%3D)
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 1959
bin: 3.75e1
variant carriers: 4

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 571
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1498
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 252
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9318
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 17175
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 6.25e1
variant carriers: 2

GenotypeDepth
all individuals: 1268
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 54
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 713
bin: 4.25e1
variant carriers: 3

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 27675
bin: 2.75e1
variant carriers: 5

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

GenotypeQuality
all individuals: 69
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2233
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1502
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7448
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 620
bin: 9.75e1
variant carriers: 21

GenotypeQuality
all individuals: 140
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 773
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44270
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1787
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

South Asian
type: Population
allele count: 17
allele frequency: 1.137123745819398e-3
allele num: 14950
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.068881808526779e-5
allele num: 65910
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10256
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.097e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.856e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.76e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.78e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

DP
type: SiteQuality
SIO_000300: 1.587845e6

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465760
ensembl transcript: ENST00000587107
gene symbol: ZBTB7C
hgvsc: ENST00000587107.1:c.30C>T
hgvsp: ENST00000587107.1:c.30C>T(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468814
ensembl transcript: ENST00000588149
gene symbol: ZBTB7C
hgvsc: ENST00000588149.1:c.30C>T
hgvsp: ENST00000588149.1:c.30C>T(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467147
ensembl transcript: ENST00000589077
gene symbol: ZBTB7C
hgvsc: ENST00000589077.1:c.30C>T
hgvsp: ENST00000589077.1:c.30C>T(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468502
ensembl transcript: ENST00000588970
gene symbol: ZBTB7C
hgvsc: ENST00000588970.1:c.30C>T
hgvsp: ENST00000588970.1:c.30C>T(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465835
ensembl transcript: ENST00000592387
gene symbol: ZBTB7C
hgvsc: ENST00000592387.1:c.30C>T
hgvsp: ENST00000592387.1:c.30C>T(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467758
ensembl transcript: ENST00000591405
gene symbol: ZBTB7C
hgvsc: ENST00000591405.1:c.30C>T
hgvsp: ENST00000591405.1:c.30C>T(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468152
ensembl transcript: ENST00000588028
gene symbol: ZBTB7C
hgvsc: ENST00000588028.1:c.30C>T
hgvsp: ENST00000588028.1:c.30C>T(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466006
ensembl transcript: ENST00000586743
gene symbol: ZBTB7C
hgvsc: ENST00000586743.1:c.30C>T
hgvsp: ENST00000586743.1:c.30C>T(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000464724
ensembl transcript: ENST00000585404
gene symbol: ZBTB7C
hgvsc: ENST00000585404.1:c.30C>T
hgvsp: ENST00000585404.1:c.30C>T(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467323
ensembl transcript: ENST00000590437
gene symbol: ZBTB7C
hgvsc: ENST00000590437.1:c.30C>T
hgvsp: ENST00000590437.1:c.30C>T(p.%3D)
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 251
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2038
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9234
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1713
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 92
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 696
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1951
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16739
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27061
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 710
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1493
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3029
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1749
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43238
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 599
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 107
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 768
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14276
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523414886810274e-5
allele num: 65642
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.570002e6

QD
type: SiteQuality
SIO_000300: 1.038e1

VQSLOD
type: SiteQuality
SIO_000300: -1.568e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.399999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.49e-1

MQ
type: SiteQuality
SIO_000300: 5.778e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465494
ensembl transcript: ENST00000590374
gene symbol: ZBTB7C
hgvsc: ENST00000590374.1:c.26T>C
hgvsp: ENSP00000465494.1:p.Ile9Thr
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467147
ensembl transcript: ENST00000589077
gene symbol: ZBTB7C
hgvsc: ENST00000589077.1:c.26T>C
hgvsp: ENSP00000467147.1:p.Ile9Thr
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468659
ensembl transcript: ENST00000589619
gene symbol: ZBTB7C
hgvsc: ENST00000589619.1:c.26T>C
hgvsp: ENSP00000468659.1:p.Ile9Thr
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000464724
ensembl transcript: ENST00000585404
gene symbol: ZBTB7C
hgvsc: ENST00000585404.1:c.26T>C
hgvsp: ENSP00000464724.1:p.Ile9Thr
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000439781
ensembl transcript: ENST00000535628
gene symbol: ZBTB7C
hgvsc: ENST00000535628.2:c.26T>C
hgvsp: ENSP00000439781.1:p.Ile9Thr
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465760
ensembl transcript: ENST00000587107
gene symbol: ZBTB7C
hgvsc: ENST00000587107.1:c.26T>C
hgvsp: ENSP00000465760.1:p.Ile9Thr
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467877
ensembl transcript: ENST00000590800
gene symbol: ZBTB7C
hgvsc: ENST00000590800.1:c.26T>C
hgvsp: ENSP00000467877.1:p.Ile9Thr
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465160
ensembl transcript: ENST00000590178
gene symbol: ZBTB7C
hgvsc: ENST00000590178.1:c.26T>C
hgvsp: ENSP00000465160.1:p.Ile9Thr
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000328732
ensembl transcript: ENST00000332053
gene symbol: ZBTB7C
hgvsc: ENST00000332053.2:c.26T>C
hgvsp: ENSP00000328732.2:p.Ile9Thr
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465835
ensembl transcript: ENST00000592387
gene symbol: ZBTB7C
hgvsc: ENST00000592387.1:c.26T>C
hgvsp: ENSP00000465835.1:p.Ile9Thr
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 672
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 2.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 26864
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1947
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 707
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1874
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2228
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16666
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 251
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9163
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3308
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 598
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 7280
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43011
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 763
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1736
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1479
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14028
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.050826774055769e-5
allele num: 65556
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.99e-1

DP
type: SiteQuality
SIO_000300: 1.563648e6

MQRankSum
type: SiteQuality
SIO_000300: -2.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.54e-1

FS
type: SiteQuality
SIO_000300: 8.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 1.531e1

VQSLOD
type: SiteQuality
SIO_000300: 5.11e-1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466944
ensembl transcript: ENST00000586047
gene symbol: ZBTB7C
hgvsc: ENST00000586047.1:c.14T>C
hgvsp: ENSP00000466944.1:p.Ile5Thr
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467147
ensembl transcript: ENST00000589077
gene symbol: ZBTB7C
hgvsc: ENST00000589077.1:c.14T>C
hgvsp: ENSP00000467147.1:p.Ile5Thr
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000439781
ensembl transcript: ENST00000535628
gene symbol: ZBTB7C
hgvsc: ENST00000535628.2:c.14T>C
hgvsp: ENSP00000439781.1:p.Ile5Thr
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000464724
ensembl transcript: ENST00000585404
gene symbol: ZBTB7C
hgvsc: ENST00000585404.1:c.14T>C
hgvsp: ENSP00000464724.1:p.Ile5Thr
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468814
ensembl transcript: ENST00000588149
gene symbol: ZBTB7C
hgvsc: ENST00000588149.1:c.14T>C
hgvsp: ENSP00000468814.1:p.Ile5Thr
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466088
ensembl transcript: ENST00000588053
gene symbol: ZBTB7C
hgvsc: ENST00000588053.1:c.14T>C
hgvsp: ENSP00000466088.1:p.Ile5Thr
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467323
ensembl transcript: ENST00000590437
gene symbol: ZBTB7C
hgvsc: ENST00000590437.1:c.14T>C
hgvsp: ENSP00000467323.1:p.Ile5Thr
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468659
ensembl transcript: ENST00000589619
gene symbol: ZBTB7C
hgvsc: ENST00000589619.1:c.14T>C
hgvsp: ENSP00000468659.1:p.Ile5Thr
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467456
ensembl transcript: ENST00000588566
gene symbol: ZBTB7C
hgvsc: ENST00000588566.1:c.14T>C
hgvsp: ENSP00000467456.1:p.Ile5Thr
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000328732
ensembl transcript: ENST00000332053
gene symbol: ZBTB7C
hgvsc: ENST00000332053.2:c.14T>C
hgvsp: ENSP00000328732.2:p.Ile5Thr
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 236
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 703
bin: 4.25e1
variant carriers: 3

GenotypeDepth
all individuals: 252
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1935
bin: 3.75e1
variant carriers: 2

GenotypeDepth
all individuals: 2766
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9065
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5
bin: 7.75e1
variant carriers: 2

GenotypeDepth
all individuals: 2397
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 12
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 29
bin: 6.25e1
variant carriers: 2

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 110
bin: 5.25e1
variant carriers: 5

GenotypeDepth
all individuals: 16108
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 4

GenotypeDepth
all individuals: 670
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26330
bin: 2.75e1
variant carriers: 2

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 102
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42048
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4113
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1467
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 579
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 9.75e1
variant carriers: 29

GenotypeQuality
all individuals: 121
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 759
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7137
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1698
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 13
allele frequency: 1.133589117544472e-3
allele num: 11468
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.275485436893204e-4
allele num: 13184
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.687271834831426e-4
allele num: 65194
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10198
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.16822429906542e-3
allele num: 856
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.6e-2

QD
type: SiteQuality
SIO_000300: 1.264e1

MQRankSum
type: SiteQuality
SIO_000300: 4.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.99e0

VQSLOD
type: SiteQuality
SIO_000300: 2.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQ
type: SiteQuality
SIO_000300: 5.955e1

DP
type: SiteQuality
SIO_000300: 1.545261e6

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465160
ensembl transcript: ENST00000590178
gene symbol: ZBTB7C
hgvsc: ENST00000590178.1:c.9T>C
hgvsp: ENST00000590178.1:c.9T>C(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467338
ensembl transcript: ENST00000589170
gene symbol: ZBTB7C
hgvsc: ENST00000589170.1:c.9T>C
hgvsp: ENST00000589170.1:c.9T>C(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465760
ensembl transcript: ENST00000587107
gene symbol: ZBTB7C
hgvsc: ENST00000587107.1:c.9T>C
hgvsp: ENST00000587107.1:c.9T>C(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467758
ensembl transcript: ENST00000591405
gene symbol: ZBTB7C
hgvsc: ENST00000591405.1:c.9T>C
hgvsp: ENST00000591405.1:c.9T>C(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466006
ensembl transcript: ENST00000586743
gene symbol: ZBTB7C
hgvsc: ENST00000586743.1:c.9T>C
hgvsp: ENST00000586743.1:c.9T>C(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468814
ensembl transcript: ENST00000588149
gene symbol: ZBTB7C
hgvsc: ENST00000588149.1:c.9T>C
hgvsp: ENST00000588149.1:c.9T>C(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467323
ensembl transcript: ENST00000590437
gene symbol: ZBTB7C
hgvsc: ENST00000590437.1:c.9T>C
hgvsp: ENST00000590437.1:c.9T>C(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000328732
ensembl transcript: ENST00000332053
gene symbol: ZBTB7C
hgvsc: ENST00000332053.2:c.9T>C
hgvsp: ENST00000332053.2:c.9T>C(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468019
ensembl transcript: ENST00000589194
gene symbol: ZBTB7C
hgvsc: ENST00000589194.1:c.9T>C
hgvsp: ENST00000589194.1:c.9T>C(p.%3D)
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465265
ensembl transcript: ENST00000591279
gene symbol: ZBTB7C
hgvsc: ENST00000591279.1:c.9T>C
hgvsp: ENST00000591279.1:c.9T>C(p.%3D)
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 251
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9044
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2585
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26082
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1930
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2923
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 15982
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 318
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 664
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 700
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1466
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7103
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41741
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4339
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 64
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 269
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 277
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1690
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.552795031055901e-4
allele num: 12880
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64990
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10176
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.8e-1

DP
type: SiteQuality
SIO_000300: 1.536782e6

MQRankSum
type: SiteQuality
SIO_000300: 3.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.5e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.56e0

QD
type: SiteQuality
SIO_000300: 1.915e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: start_lost
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468659
ensembl transcript: ENST00000589619
gene symbol: ZBTB7C
hgvsc: ENST00000589619.1:c.2T>C
hgvsp: ENSP00000468659.1:p.Met1?
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: start_lost
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000464724
ensembl transcript: ENST00000585404
gene symbol: ZBTB7C
hgvsc: ENST00000585404.1:c.2T>C
hgvsp: ENSP00000464724.1:p.Met1?
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: start_lost
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468019
ensembl transcript: ENST00000589194
gene symbol: ZBTB7C
hgvsc: ENST00000589194.1:c.2T>C
hgvsp: ENSP00000468019.1:p.Met1?
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: start_lost
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466944
ensembl transcript: ENST00000586047
gene symbol: ZBTB7C
hgvsc: ENST00000586047.1:c.2T>C
hgvsp: ENSP00000466944.1:p.Met1?
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: start_lost
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468814
ensembl transcript: ENST00000588149
gene symbol: ZBTB7C
hgvsc: ENST00000588149.1:c.2T>C
hgvsp: ENSP00000468814.1:p.Met1?
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: start_lost
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468537
ensembl transcript: ENST00000586525
gene symbol: ZBTB7C
hgvsc: ENST00000586525.1:c.2T>C
hgvsp: ENSP00000468537.1:p.Met1?
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: start_lost
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465160
ensembl transcript: ENST00000590178
gene symbol: ZBTB7C
hgvsc: ENST00000590178.1:c.2T>C
hgvsp: ENSP00000465160.1:p.Met1?
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: start_lost
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468152
ensembl transcript: ENST00000588028
gene symbol: ZBTB7C
hgvsc: ENST00000588028.1:c.2T>C
hgvsp: ENSP00000468152.1:p.Met1?
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: start_lost
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465760
ensembl transcript: ENST00000587107
gene symbol: ZBTB7C
hgvsc: ENST00000587107.1:c.2T>C
hgvsp: ENSP00000465760.1:p.Met1?
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: start_lost
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468087
ensembl transcript: ENST00000592656
gene symbol: ZBTB7C
hgvsc: ENST00000592656.1:c.2T>C
hgvsp: ENSP00000468087.1:p.Met1?
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 575
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3041
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 698
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25798
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 664
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8977
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2850
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15700
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 251
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1918
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7050
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1659
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1447
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 751
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4604
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41109
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 266
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.545977366891349e-5
allele num: 64684
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12268
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10124
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -6.332e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQ
type: SiteQuality
SIO_000300: 5.951e1

DP
type: SiteQuality
SIO_000300: 1.524336e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.85e-1

FS
type: SiteQuality
SIO_000300: 4.872e0

MQRankSum
type: SiteQuality
SIO_000300: -1.366e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-2

QD
type: SiteQuality
SIO_000300: 9.34e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.8e-1

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467456
ensembl transcript: ENST00000588566
gene symbol: ZBTB7C
hgvsc: ENST00000588566.1:c.-9_-6delGCTG
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468254
ensembl transcript: ENST00000586438
gene symbol: ZBTB7C
hgvsc: ENST00000586438.1:c.-9_-6delGCTG
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467323
ensembl transcript: ENST00000590437
gene symbol: ZBTB7C
hgvsc: ENST00000590437.1:c.-9_-6delGCTG
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466088
ensembl transcript: ENST00000588053
gene symbol: ZBTB7C
hgvsc: ENST00000588053.1:c.-9_-6delGCTG
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465160
ensembl transcript: ENST00000590178
gene symbol: ZBTB7C
hgvsc: ENST00000590178.1:c.-9_-6delGCTG
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468152
ensembl transcript: ENST00000588028
gene symbol: ZBTB7C
hgvsc: ENST00000588028.1:c.-9_-6delGCTG
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000464724
ensembl transcript: ENST00000585404
gene symbol: ZBTB7C
hgvsc: ENST00000585404.1:c.-9_-6delGCTG
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468814
ensembl transcript: ENST00000588149
gene symbol: ZBTB7C
hgvsc: ENST00000588149.1:c.-9_-6delGCTG
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 8930
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3178
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3030
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 729
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 251
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 697
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 823
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 25488
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1918
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15415
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 745
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 881
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4750
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40471
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1646
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 703
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1427
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7022
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 218
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 1.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11408
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.552843256001739e-5
allele num: 64398
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11788
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.512996e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

QD
type: SiteQuality
SIO_000300: 1.196e1

MQ
type: SiteQuality
SIO_000300: 5.634e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.86e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.07e0

FS
type: SiteQuality
SIO_000300: 1.207e0

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.39e-1

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465494
ensembl transcript: ENST00000590374
gene symbol: ZBTB7C
hgvsc: ENST00000590374.1:c.-13T>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465160
ensembl transcript: ENST00000590178
gene symbol: ZBTB7C
hgvsc: ENST00000590178.1:c.-13T>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000328732
ensembl transcript: ENST00000332053
gene symbol: ZBTB7C
hgvsc: ENST00000332053.2:c.-13T>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468152
ensembl transcript: ENST00000588028
gene symbol: ZBTB7C
hgvsc: ENST00000588028.1:c.-13T>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468254
ensembl transcript: ENST00000586438
gene symbol: ZBTB7C
hgvsc: ENST00000586438.1:c.-13T>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000464724
ensembl transcript: ENST00000585404
gene symbol: ZBTB7C
hgvsc: ENST00000585404.1:c.-13T>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465760
ensembl transcript: ENST00000587107
gene symbol: ZBTB7C
hgvsc: ENST00000587107.1:c.-13T>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467456
ensembl transcript: ENST00000588566
gene symbol: ZBTB7C
hgvsc: ENST00000588566.1:c.-13T>G
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 3349
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1899
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14830
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24861
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3556
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1341
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 251
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 696
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 27
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8772
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 880
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39130
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1567
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 784
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1430
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1388
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6723
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5136
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8520
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11370
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6448
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.56710336613803e-5
allele num: 63812
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9912
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-2

FS
type: SiteQuality
SIO_000300: 4.041e0

QD
type: SiteQuality
SIO_000300: 8.109999999999999e0

MQ
type: SiteQuality
SIO_000300: 5.957e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

DP
type: SiteQuality
SIO_000300: 1.487879e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.575e0

MQRankSum
type: SiteQuality
SIO_000300: 1.87e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -8.156e-1

Annotation
canonical: false
consequence: splice_region_variant
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468752
ensembl transcript: ENST00000591526
gene symbol: ZBTB7C
hgvsc: ENST00000591526.1:c.-16G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: splice_region_variant
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000464724
ensembl transcript: ENST00000585404
gene symbol: ZBTB7C
hgvsc: ENST00000585404.1:c.-16G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: splice_region_variant
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468502
ensembl transcript: ENST00000588970
gene symbol: ZBTB7C
hgvsc: ENST00000588970.1:c.-16G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: splice_region_variant
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467323
ensembl transcript: ENST00000590437
gene symbol: ZBTB7C
hgvsc: ENST00000590437.1:c.-16G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: splice_region_variant
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468019
ensembl transcript: ENST00000589194
gene symbol: ZBTB7C
hgvsc: ENST00000589194.1:c.-16G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: splice_region_variant
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465760
ensembl transcript: ENST00000587107
gene symbol: ZBTB7C
hgvsc: ENST00000587107.1:c.-16G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: splice_region_variant
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468254
ensembl transcript: ENST00000586438
gene symbol: ZBTB7C
hgvsc: ENST00000586438.1:c.-16G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: splice_region_variant
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467758
ensembl transcript: ENST00000591405
gene symbol: ZBTB7C
hgvsc: ENST00000591405.1:c.-16G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: splice_region_variant
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468537
ensembl transcript: ENST00000586525
gene symbol: ZBTB7C
hgvsc: ENST00000586525.1:c.-16G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: splice_region_variant
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468152
ensembl transcript: ENST00000588028
gene symbol: ZBTB7C
hgvsc: ENST00000588028.1:c.-16G>C
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 3400
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8698
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14728
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1896
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 252
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3647
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1462
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 888
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24767
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 693
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1572
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39117
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5264
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6687
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1548
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 798
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1361
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10730
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.011736139214893e-4
allele num: 9884
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.19e-1

FS
type: SiteQuality
SIO_000300: 4.182e0

MQRankSum
type: SiteQuality
SIO_000300: 2.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.169999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

QD
type: SiteQuality
SIO_000300: 1.549e1

DP
type: SiteQuality
SIO_000300: 1.482559e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.49e0

Annotation
canonical: false
consequence: splice_acceptor_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467338
ensembl transcript: ENST00000589170
gene symbol: ZBTB7C
hgvsc: ENST00000589170.1:c.-16-2A>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: splice_acceptor_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468537
ensembl transcript: ENST00000586525
gene symbol: ZBTB7C
hgvsc: ENST00000586525.1:c.-16-2A>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: splice_acceptor_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467147
ensembl transcript: ENST00000589077
gene symbol: ZBTB7C
hgvsc: ENST00000589077.1:c.-16-2A>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: splice_acceptor_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467323
ensembl transcript: ENST00000590437
gene symbol: ZBTB7C
hgvsc: ENST00000590437.1:c.-16-2A>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: splice_acceptor_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468254
ensembl transcript: ENST00000586438
gene symbol: ZBTB7C
hgvsc: ENST00000586438.1:c.-16-2A>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: splice_acceptor_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465835
ensembl transcript: ENST00000592387
gene symbol: ZBTB7C
hgvsc: ENST00000592387.1:c.-16-2A>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: splice_acceptor_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468814
ensembl transcript: ENST00000588149
gene symbol: ZBTB7C
hgvsc: ENST00000588149.1:c.-16-2A>G
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 27
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3723
bin: 1.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 902
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1885
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3445
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 24690
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8681
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 694
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1520
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14635
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 254
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 721
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 732
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1540
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1347
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1633
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5404
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 802
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6684
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39138
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63584
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9876
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10634
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.762114537444934e-4
allele num: 11350
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6432
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.65e0

VQSLOD
type: SiteQuality
SIO_000300: -9.717e-1

FS
type: SiteQuality
SIO_000300: 2.462e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.41e0

DP
type: SiteQuality
SIO_000300: 1.479221e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.31e-1

QD
type: SiteQuality
SIO_000300: 1.28e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.39e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000439781
ensembl transcript: ENST00000535628
gene symbol: ZBTB7C
hgvsc: ENST00000535628.2:c.-16-8C>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468087
ensembl transcript: ENST00000592656
gene symbol: ZBTB7C
hgvsc: ENST00000592656.1:c.-16-8C>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465160
ensembl transcript: ENST00000590178
gene symbol: ZBTB7C
hgvsc: ENST00000590178.1:c.-16-8C>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465265
ensembl transcript: ENST00000591279
gene symbol: ZBTB7C
hgvsc: ENST00000591279.1:c.-16-8C>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468814
ensembl transcript: ENST00000588149
gene symbol: ZBTB7C
hgvsc: ENST00000588149.1:c.-16-8C>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467323
ensembl transcript: ENST00000590437
gene symbol: ZBTB7C
hgvsc: ENST00000590437.1:c.-16-8C>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466006
ensembl transcript: ENST00000586743
gene symbol: ZBTB7C
hgvsc: ENST00000586743.1:c.-16-8C>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468659
ensembl transcript: ENST00000589619
gene symbol: ZBTB7C
hgvsc: ENST00000589619.1:c.-16-8C>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467338
ensembl transcript: ENST00000589170
gene symbol: ZBTB7C
hgvsc: ENST00000589170.1:c.-16-8C>G
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 1184
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3547
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2033
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1855
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 4367
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8461
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23808
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 250
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14203
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 689
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1430
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 951
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5783
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2150
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6167
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1286
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37612
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9774
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11318
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.584434515321482e-5
allele num: 63114
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.84e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.77e0

QD
type: SiteQuality
SIO_000300: 1.504e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

DP
type: SiteQuality
SIO_000300: 1.451881e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.9e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.95e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466006
ensembl transcript: ENST00000586743
gene symbol: ZBTB7C
hgvsc: ENST00000586743.1:c.-16-10G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465760
ensembl transcript: ENST00000587107
gene symbol: ZBTB7C
hgvsc: ENST00000587107.1:c.-16-10G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467323
ensembl transcript: ENST00000590437
gene symbol: ZBTB7C
hgvsc: ENST00000590437.1:c.-16-10G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468254
ensembl transcript: ENST00000586438
gene symbol: ZBTB7C
hgvsc: ENST00000586438.1:c.-16-10G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468537
ensembl transcript: ENST00000586525
gene symbol: ZBTB7C
hgvsc: ENST00000586525.1:c.-16-10G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468814
ensembl transcript: ENST00000588149
gene symbol: ZBTB7C
hgvsc: ENST00000588149.1:c.-16-10G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465494
ensembl transcript: ENST00000590374
gene symbol: ZBTB7C
hgvsc: ENST00000590374.1:c.-16-10G>C
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4358
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 250
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 688
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1164
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1853
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 106
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 27
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23780
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3566
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2044
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14271
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8422
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5850
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 926
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38007
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 166
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2167
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6145
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 936
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1414
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1280
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 706
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6394
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10004
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.755865567533291e-5
allele num: 63080
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11314
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.03e-1

QD
type: SiteQuality
SIO_000300: 1.007e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.28e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.61e-1

DP
type: SiteQuality
SIO_000300: 1.451104e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.84e-1

FS
type: SiteQuality
SIO_000300: 4.3e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.337e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000464724
ensembl transcript: ENST00000585404
gene symbol: ZBTB7C
hgvsc: ENST00000585404.1:c.-16-11T>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465835
ensembl transcript: ENST00000592387
gene symbol: ZBTB7C
hgvsc: ENST00000592387.1:c.-16-11T>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466006
ensembl transcript: ENST00000586743
gene symbol: ZBTB7C
hgvsc: ENST00000586743.1:c.-16-11T>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465760
ensembl transcript: ENST00000587107
gene symbol: ZBTB7C
hgvsc: ENST00000587107.1:c.-16-11T>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467758
ensembl transcript: ENST00000591405
gene symbol: ZBTB7C
hgvsc: ENST00000591405.1:c.-16-11T>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468659
ensembl transcript: ENST00000589619
gene symbol: ZBTB7C
hgvsc: ENST00000589619.1:c.-16-11T>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467456
ensembl transcript: ENST00000588566
gene symbol: ZBTB7C
hgvsc: ENST00000588566.1:c.-16-11T>G
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 23658
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14176
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 249
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 8384
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 1218
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4493
bin: 1.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 2106
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1850
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3565
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 690
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 977
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 961
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37777
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5945
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2236
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1411
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6121
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1274
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 5.75e1
variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 9.213759213759214e-4
allele num: 9768
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11314
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63044
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9960
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.01e-1

QD
type: SiteQuality
SIO_000300: 1.193e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.52e0

FS
type: SiteQuality
SIO_000300: 8.070000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.95e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.41e-1

DP
type: SiteQuality
SIO_000300: 1.447178e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468814
ensembl transcript: ENST00000588149
gene symbol: ZBTB7C
hgvsc: ENST00000588149.1:c.-16-14G>A
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466006
ensembl transcript: ENST00000586743
gene symbol: ZBTB7C
hgvsc: ENST00000586743.1:c.-16-14G>A
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468152
ensembl transcript: ENST00000588028
gene symbol: ZBTB7C
hgvsc: ENST00000588028.1:c.-16-14G>A
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468019
ensembl transcript: ENST00000589194
gene symbol: ZBTB7C
hgvsc: ENST00000589194.1:c.-16-14G>A
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468752
ensembl transcript: ENST00000591526
gene symbol: ZBTB7C
hgvsc: ENST00000591526.1:c.-16-14G>A
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468254
ensembl transcript: ENST00000586438
gene symbol: ZBTB7C
hgvsc: ENST00000586438.1:c.-16-14G>A
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000439781
ensembl transcript: ENST00000535628
gene symbol: ZBTB7C
hgvsc: ENST00000535628.2:c.-16-14G>A
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 13716
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3543
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2316
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1431
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23257
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4976
bin: 1.25e1
variant carriers: 2

GenotypeDepth
all individuals: 1853
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8349
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 247
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 686
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6016
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1161
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1075
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6216
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2457
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1378
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1242
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 37054
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 1.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9728
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62884
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6374
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 4.091653027823241e-4
allele num: 9776
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11282
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.183431952662722e-4
allele num: 8450
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.389999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.434631e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.664e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

FS
type: SiteQuality
SIO_000300: 4.048e0

QD
type: SiteQuality
SIO_000300: 1.242e1

MQRankSum
type: SiteQuality
SIO_000300: -1.94e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-2

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467877
ensembl transcript: ENST00000590800
gene symbol: ZBTB7C
hgvsc: ENST00000590800.1:c.-16-16C>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468502
ensembl transcript: ENST00000588970
gene symbol: ZBTB7C
hgvsc: ENST00000588970.1:c.-16-16C>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468306
ensembl transcript: ENST00000590855
gene symbol: ZBTB7C
hgvsc: ENST00000590855.1:c.-16-16C>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465835
ensembl transcript: ENST00000592387
gene symbol: ZBTB7C
hgvsc: ENST00000592387.1:c.-16-16C>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465265
ensembl transcript: ENST00000591279
gene symbol: ZBTB7C
hgvsc: ENST00000591279.1:c.-16-16C>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467758
ensembl transcript: ENST00000591405
gene symbol: ZBTB7C
hgvsc: ENST00000591405.1:c.-16-16C>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468152
ensembl transcript: ENST00000588028
gene symbol: ZBTB7C
hgvsc: ENST00000588028.1:c.-16-16C>G
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 246
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22930
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5351
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2443
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3541
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1631
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13426
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 688
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8258
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1851
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 237
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1348
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5956
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 227
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1166
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1225
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2603
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1286
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6522
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36513
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9700
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8438
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9722
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62778
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.570845114671693e-4
allele num: 6366
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 1.406e1

FS
type: SiteQuality
SIO_000300: 8.087e0

MQRankSum
type: SiteQuality
SIO_000300: -5.79e-1

MQ
type: SiteQuality
SIO_000300: 5.806e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.88e-1

DP
type: SiteQuality
SIO_000300: 1.424512e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467323
ensembl transcript: ENST00000590437
gene symbol: ZBTB7C
hgvsc: ENST00000590437.1:c.-16-19_-16-17delTCT
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465835
ensembl transcript: ENST00000592387
gene symbol: ZBTB7C
hgvsc: ENST00000592387.1:c.-16-19_-16-17delTCT
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467456
ensembl transcript: ENST00000588566
gene symbol: ZBTB7C
hgvsc: ENST00000588566.1:c.-16-19_-16-17delTCT
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466088
ensembl transcript: ENST00000588053
gene symbol: ZBTB7C
hgvsc: ENST00000588053.1:c.-16-19_-16-17delTCT
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467338
ensembl transcript: ENST00000589170
gene symbol: ZBTB7C
hgvsc: ENST00000589170.1:c.-16-19_-16-17delTCT
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468502
ensembl transcript: ENST00000588970
gene symbol: ZBTB7C
hgvsc: ENST00000588970.1:c.-16-19_-16-17delTCT
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465160
ensembl transcript: ENST00000590178
gene symbol: ZBTB7C
hgvsc: ENST00000590178.1:c.-16-19_-16-17delTCT
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 27
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1631
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13426
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22930
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8258
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1851
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2443
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3541
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 688
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5351
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 246
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1348
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1225
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6522
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1166
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1286
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2603
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36513
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5956
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9722
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62778
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.869966294128082e-5
allele num: 11274
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9700
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6366
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.424512e6

MQRankSum
type: SiteQuality
SIO_000300: -5.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.79e-1

FS
type: SiteQuality
SIO_000300: 8.087e0

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

QD
type: SiteQuality
SIO_000300: 1.406e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

MQ
type: SiteQuality
SIO_000300: 5.806e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.88e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465832
ensembl transcript: ENST00000593159
gene symbol: ZBTB7C
hgvsc: ENST00000593159.1:c.-16-18C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465835
ensembl transcript: ENST00000592387
gene symbol: ZBTB7C
hgvsc: ENST00000592387.1:c.-16-18C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467456
ensembl transcript: ENST00000588566
gene symbol: ZBTB7C
hgvsc: ENST00000588566.1:c.-16-18C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000464724
ensembl transcript: ENST00000585404
gene symbol: ZBTB7C
hgvsc: ENST00000585404.1:c.-16-18C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467323
ensembl transcript: ENST00000590437
gene symbol: ZBTB7C
hgvsc: ENST00000590437.1:c.-16-18C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468502
ensembl transcript: ENST00000588970
gene symbol: ZBTB7C
hgvsc: ENST00000588970.1:c.-16-18C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468019
ensembl transcript: ENST00000589194
gene symbol: ZBTB7C
hgvsc: ENST00000589194.1:c.-16-18C>T
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3519
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8204
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2610
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1846
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12809
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5951
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2073
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22392
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 687
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 246
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1337
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1330
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2781
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1211
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1521
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5860
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 316
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 680
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6902
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35174
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6354
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9648
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11258
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.187648456057007e-4
allele num: 8420
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62626
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.0e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.424e-1

QD
type: SiteQuality
SIO_000300: 8.369999999999999e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.798e0

FS
type: SiteQuality
SIO_000300: 2.17e0

MQRankSum
type: SiteQuality
SIO_000300: -6.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

DP
type: SiteQuality
SIO_000300: 1.409309e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000439781
ensembl transcript: ENST00000535628
gene symbol: ZBTB7C
hgvsc: ENST00000535628.2:c.-16-22T>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466006
ensembl transcript: ENST00000586743
gene symbol: ZBTB7C
hgvsc: ENST00000586743.1:c.-16-22T>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467323
ensembl transcript: ENST00000590437
gene symbol: ZBTB7C
hgvsc: ENST00000590437.1:c.-16-22T>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465160
ensembl transcript: ENST00000590178
gene symbol: ZBTB7C
hgvsc: ENST00000590178.1:c.-16-22T>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468087
ensembl transcript: ENST00000592656
gene symbol: ZBTB7C
hgvsc: ENST00000592656.1:c.-16-22T>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465832
ensembl transcript: ENST00000593159
gene symbol: ZBTB7C
hgvsc: ENST00000593159.1:c.-16-22T>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467338
ensembl transcript: ENST00000589170
gene symbol: ZBTB7C
hgvsc: ENST00000589170.1:c.-16-22T>C
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 1838
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2800
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2783
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 245
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3515
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6834
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 686
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 8088
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11895
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 21632
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1311
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1983
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5790
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3022
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 224
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7442
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1188
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1608
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 239
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 674
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33817
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.202049311559398e-5
allele num: 62460
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11240
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 758
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6344
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.66e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.54e0

FS
type: SiteQuality
SIO_000300: 1.362e0

MQRankSum
type: SiteQuality
SIO_000300: 7.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -5.32e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.24e0

DP
type: SiteQuality
SIO_000300: 1.387513e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465835
ensembl transcript: ENST00000592387
gene symbol: ZBTB7C
hgvsc: ENST00000592387.1:c.-16-23T>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468152
ensembl transcript: ENST00000588028
gene symbol: ZBTB7C
hgvsc: ENST00000588028.1:c.-16-23T>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468019
ensembl transcript: ENST00000589194
gene symbol: ZBTB7C
hgvsc: ENST00000589194.1:c.-16-23T>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467338
ensembl transcript: ENST00000589170
gene symbol: ZBTB7C
hgvsc: ENST00000589170.1:c.-16-23T>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465160
ensembl transcript: ENST00000590178
gene symbol: ZBTB7C
hgvsc: ENST00000590178.1:c.-16-23T>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000464724
ensembl transcript: ENST00000585404
gene symbol: ZBTB7C
hgvsc: ENST00000585404.1:c.-16-23T>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467323
ensembl transcript: ENST00000590437
gene symbol: ZBTB7C
hgvsc: ENST00000590437.1:c.-16-23T>G
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 10769
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3454
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 686
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2982
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1832
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7935
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7958
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20522
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 245
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3901
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31061
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7903
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1485
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3231
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1988
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1172
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2594
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5458
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 583
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 677
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 695
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1280
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6324
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.045369015262388e-4
allele num: 9566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11236
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 754
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62316
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8380
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9374
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

VQSLOD
type: SiteQuality
SIO_000300: 7.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.171e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

QD
type: SiteQuality
SIO_000300: 1.351e1

DP
type: SiteQuality
SIO_000300: 1.360546e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468659
ensembl transcript: ENST00000589619
gene symbol: ZBTB7C
hgvsc: ENST00000589619.1:c.-16-41_-16-38delACGC
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468019
ensembl transcript: ENST00000589194
gene symbol: ZBTB7C
hgvsc: ENST00000589194.1:c.-16-41_-16-38delACGC
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468814
ensembl transcript: ENST00000588149
gene symbol: ZBTB7C
hgvsc: ENST00000588149.1:c.-16-41_-16-38delACGC
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468537
ensembl transcript: ENST00000586525
gene symbol: ZBTB7C
hgvsc: ENST00000586525.1:c.-16-41_-16-38delACGC
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468254
ensembl transcript: ENST00000586438
gene symbol: ZBTB7C
hgvsc: ENST00000586438.1:c.-16-41_-16-38delACGC
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466944
ensembl transcript: ENST00000586047
gene symbol: ZBTB7C
hgvsc: ENST00000586047.1:c.-16-41_-16-38delACGC
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467758
ensembl transcript: ENST00000591405
gene symbol: ZBTB7C
hgvsc: ENST00000591405.1:c.-16-41_-16-38delACGC
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 613
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3724
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3472
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1495
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12647
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14005
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10539
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8011
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 236
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5254
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1991
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6100
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3869
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1935
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3717
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 746
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1011
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9867
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1030
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3519
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5230
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17503
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 742
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6246
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8126
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8954
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61342
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11106
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8754
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

QD
type: SiteQuality
SIO_000300: 4.09e0

VQSLOD
type: SiteQuality
SIO_000300: -5.79e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 9.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQRankSum
type: SiteQuality
SIO_000300: -1.92e0

MQ
type: SiteQuality
SIO_000300: 5.065e1

DP
type: SiteQuality
SIO_000300: 1.190561e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465160
ensembl transcript: ENST00000590178
gene symbol: ZBTB7C
hgvsc: ENST00000590178.1:c.-16-40C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468537
ensembl transcript: ENST00000586525
gene symbol: ZBTB7C
hgvsc: ENST00000586525.1:c.-16-40C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467456
ensembl transcript: ENST00000588566
gene symbol: ZBTB7C
hgvsc: ENST00000588566.1:c.-16-40C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468254
ensembl transcript: ENST00000586438
gene symbol: ZBTB7C
hgvsc: ENST00000586438.1:c.-16-40C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468152
ensembl transcript: ENST00000588028
gene symbol: ZBTB7C
hgvsc: ENST00000588028.1:c.-16-40C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465265
ensembl transcript: ENST00000591279
gene symbol: ZBTB7C
hgvsc: ENST00000591279.1:c.-16-40C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467758
ensembl transcript: ENST00000591405
gene symbol: ZBTB7C
hgvsc: ENST00000591405.1:c.-16-40C>T
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 9675
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 577
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9951
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4125
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15835
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 225
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10442
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3492
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4220
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1341
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 99
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9085
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3544
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 679
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2776
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 940
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6384
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 955
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1055
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4062
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6691
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3083
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 555
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12363
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 992
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3922
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1290
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8442
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6178
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8360
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.120758847136082e-5
allele num: 10964
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60662
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7772
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.069e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.34e-1

DP
type: SiteQuality
SIO_000300: 1.146015e6

QD
type: SiteQuality
SIO_000300: 1.323e1

VQSLOD
type: SiteQuality
SIO_000300: 8.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.67e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000464724
ensembl transcript: ENST00000585404
gene symbol: ZBTB7C
hgvsc: ENST00000585404.1:c.-16-42delC
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465760
ensembl transcript: ENST00000587107
gene symbol: ZBTB7C
hgvsc: ENST00000587107.1:c.-16-42delC
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467147
ensembl transcript: ENST00000589077
gene symbol: ZBTB7C
hgvsc: ENST00000589077.1:c.-16-42delC
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466088
ensembl transcript: ENST00000588053
gene symbol: ZBTB7C
hgvsc: ENST00000588053.1:c.-16-42delC
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468537
ensembl transcript: ENST00000586525
gene symbol: ZBTB7C
hgvsc: ENST00000586525.1:c.-16-42delC
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468814
ensembl transcript: ENST00000588149
gene symbol: ZBTB7C
hgvsc: ENST00000588149.1:c.-16-42delC
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465160
ensembl transcript: ENST00000590178
gene symbol: ZBTB7C
hgvsc: ENST00000590178.1:c.-16-42delC
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 15757
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4149
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3502
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9726
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 10495
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 26
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4149
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 99
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9968
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 571
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1337
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 223
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3498
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9144
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2759
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1195
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 896
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6698
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3932
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6392
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1039
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4098
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 944
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12843
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3094
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 993
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6192
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8320
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10956
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7762
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.292506255761886e-5
allele num: 60744
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 736
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-2

MQ
type: SiteQuality
SIO_000300: 6.021e1

VQSLOD
type: SiteQuality
SIO_000300: 4.59e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

DP
type: SiteQuality
SIO_000300: 1.144428e6

QD
type: SiteQuality
SIO_000300: 1.199e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.639999999999999e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467323
ensembl transcript: ENST00000590437
gene symbol: ZBTB7C
hgvsc: ENST00000590437.1:c.-16-43C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466944
ensembl transcript: ENST00000586047
gene symbol: ZBTB7C
hgvsc: ENST00000586047.1:c.-16-43C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468752
ensembl transcript: ENST00000591526
gene symbol: ZBTB7C
hgvsc: ENST00000591526.1:c.-16-43C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465494
ensembl transcript: ENST00000590374
gene symbol: ZBTB7C
hgvsc: ENST00000590374.1:c.-16-43C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467147
ensembl transcript: ENST00000589077
gene symbol: ZBTB7C
hgvsc: ENST00000589077.1:c.-16-43C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468814
ensembl transcript: ENST00000588149
gene symbol: ZBTB7C
hgvsc: ENST00000588149.1:c.-16-43C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465160
ensembl transcript: ENST00000590178
gene symbol: ZBTB7C
hgvsc: ENST00000590178.1:c.-16-43C>T
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 1287
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4435
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 3661
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10441
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11543
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3498
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 99
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8543
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15634
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 550
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 211
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 880
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9964
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8374
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6770
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4128
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 897
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4645
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1390
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3869
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 964
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2621
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2043
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6735
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3161
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1324
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10758
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 724
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6118
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.665168015452759e-5
allele num: 60054
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7396
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7880
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 4.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -5.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.56e-1

DP
type: SiteQuality
SIO_000300: 1.126469e6

VQSLOD
type: SiteQuality
SIO_000300: -3.656e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

MQ
type: SiteQuality
SIO_000300: 5.875e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468019
ensembl transcript: ENST00000589194
gene symbol: ZBTB7C
hgvsc: ENST00000589194.1:c.-16-46G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468254
ensembl transcript: ENST00000586438
gene symbol: ZBTB7C
hgvsc: ENST00000586438.1:c.-16-46G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000464724
ensembl transcript: ENST00000585404
gene symbol: ZBTB7C
hgvsc: ENST00000585404.1:c.-16-46G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468814
ensembl transcript: ENST00000588149
gene symbol: ZBTB7C
hgvsc: ENST00000588149.1:c.-16-46G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465760
ensembl transcript: ENST00000587107
gene symbol: ZBTB7C
hgvsc: ENST00000587107.1:c.-16-46G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468502
ensembl transcript: ENST00000588970
gene symbol: ZBTB7C
hgvsc: ENST00000588970.1:c.-16-46G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468659
ensembl transcript: ENST00000589619
gene symbol: ZBTB7C
hgvsc: ENST00000589619.1:c.-16-46G>C
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 3504
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1259
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 536
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3381
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 12233
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 207
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4566
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 15453
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10502
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7815
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 96
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 962
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1043
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3272
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2121
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7369
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5297
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3830
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1512
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3808
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 890
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6865
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6762
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 263
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8363
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2506
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2913
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6808
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10522
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 712
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.676839492923737e-5
allele num: 59636
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8042
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7280
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6044
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

FS
type: SiteQuality
SIO_000300: 2.037e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.44e-1

DP
type: SiteQuality
SIO_000300: 1.116015e6

VQSLOD
type: SiteQuality
SIO_000300: 4.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.698e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466006
ensembl transcript: ENST00000586743
gene symbol: ZBTB7C
hgvsc: ENST00000586743.1:c.-85+2717C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468152
ensembl transcript: ENST00000588028
gene symbol: ZBTB7C
hgvsc: ENST00000588028.1:c.-146+23520C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467338
ensembl transcript: ENST00000589170
gene symbol: ZBTB7C
hgvsc: ENST00000589170.1:c.-17+2717C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467323
ensembl transcript: ENST00000590437
gene symbol: ZBTB7C
hgvsc: ENST00000590437.1:c.-146+2717C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465760
ensembl transcript: ENST00000587107
gene symbol: ZBTB7C
hgvsc: ENST00000587107.1:c.-17+2717C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468537
ensembl transcript: ENST00000586525
gene symbol: ZBTB7C
hgvsc: ENST00000586525.1:c.-17+2717C>T
variant of: http://identifiers.org/hgnc/31700

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

GenotypeDepth
all individuals: 10
bin: 5.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 1192
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 154
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 169
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 6.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2129
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2347
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 474
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1960
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1999
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2665
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 471
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1027
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.770083102493075e-4
allele num: 3610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.162e0

QD
type: SiteQuality
SIO_000300: 1.507e1

DP
type: SiteQuality
SIO_000300: 1.75093e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e-1

MQ
type: SiteQuality
SIO_000300: 5.838e1

VQSLOD
type: SiteQuality
SIO_000300: -1.857e0

MQRankSum
type: SiteQuality
SIO_000300: 1.81e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.25e-2

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466944
ensembl transcript: ENST00000586047
gene symbol: ZBTB7C
hgvsc: ENST00000586047.1:c.-17+23501dupA
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468659
ensembl transcript: ENST00000589619
gene symbol: ZBTB7C
hgvsc: ENST00000589619.1:c.-85+2694dupA
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465832
ensembl transcript: ENST00000593159
gene symbol: ZBTB7C
hgvsc: ENST00000593159.1:c.-85+2698dupA
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468502
ensembl transcript: ENST00000588970
gene symbol: ZBTB7C
hgvsc: ENST00000588970.1:c.-168+23501dupA
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467456
ensembl transcript: ENST00000588566
gene symbol: ZBTB7C
hgvsc: ENST00000588566.1:c.-17+23501dupA
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465760
ensembl transcript: ENST00000587107
gene symbol: ZBTB7C
hgvsc: ENST00000587107.1:c.-17+2698dupA
variant of: http://identifiers.org/hgnc/31700

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

GenotypeDepth
all individuals: 478
bin: 3.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 1197
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 4.25e1
variant carriers: 2

GenotypeDepth
all individuals: 1899
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 120
bin: 1.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 187
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1909
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 265
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2462
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 546
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1005
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 208
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 94
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1908
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2295
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3590
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 556
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 6.585879873551106e-4
allele num: 7592
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.49e-2

MQ
type: SiteQuality
SIO_000300: 6.016e1

FS
type: SiteQuality
SIO_000300: 7.82e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.76e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -9.57e-1

DP
type: SiteQuality
SIO_000300: 1.73671e5

VQSLOD
type: SiteQuality
SIO_000300: 4.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.08e-1

QD
type: SiteQuality
SIO_000300: 1.481e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468502
ensembl transcript: ENST00000588970
gene symbol: ZBTB7C
hgvsc: ENST00000588970.1:c.-168+20844G>A
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465160
ensembl transcript: ENST00000590178
gene symbol: ZBTB7C
hgvsc: ENST00000590178.1:c.-17+41G>A
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468254
ensembl transcript: ENST00000586438
gene symbol: ZBTB7C
hgvsc: ENST00000586438.1:c.-17+41G>A
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467456
ensembl transcript: ENST00000588566
gene symbol: ZBTB7C
hgvsc: ENST00000588566.1:c.-17+20844G>A
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468019
ensembl transcript: ENST00000589194
gene symbol: ZBTB7C
hgvsc: ENST00000589194.1:c.-17+15240G>A
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465760
ensembl transcript: ENST00000587107
gene symbol: ZBTB7C
hgvsc: ENST00000587107.1:c.-17+41G>A
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 1010
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1255
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2569
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 398
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 201
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2066
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 118
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 6.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1048
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 123
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1112
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1063
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 142
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1999
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.664447403462051e-4
allele num: 6008
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 110
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3170
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.265e1

VQSLOD
type: SiteQuality
SIO_000300: -5.888e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.03e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.285e0

DP
type: SiteQuality
SIO_000300: 1.10714e5

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466088
ensembl transcript: ENST00000588053
gene symbol: ZBTB7C
hgvsc: ENST00000588053.1:c.-96A>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466944
ensembl transcript: ENST00000586047
gene symbol: ZBTB7C
hgvsc: ENST00000586047.1:c.-17+20774A>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468814
ensembl transcript: ENST00000588149
gene symbol: ZBTB7C
hgvsc: ENST00000588149.1:c.-17+20164A>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465160
ensembl transcript: ENST00000590178
gene symbol: ZBTB7C
hgvsc: ENST00000590178.1:c.-46A>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468752
ensembl transcript: ENST00000591526
gene symbol: ZBTB7C
hgvsc: ENST00000591526.1:c.-96A>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468502
ensembl transcript: ENST00000588970
gene symbol: ZBTB7C
hgvsc: ENST00000588970.1:c.-168+20774A>G
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3878
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2124
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 372
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 134
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 41
bin: 4.75e1
variant carriers: 2

GenotypeDepth
all individuals: 5
bin: 1.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 122
bin: 3.75e1
variant carriers: 2

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1578
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 102
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4980
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1907
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 136
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 84
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3586
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 1.051801209571391e-3
allele num: 7606
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 5.319148936170213e-3
allele num: 188
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-2

FS
type: SiteQuality
SIO_000300: 1.3276e1

VQSLOD
type: SiteQuality
SIO_000300: -1.407e0

QD
type: SiteQuality
SIO_000300: 1.597e1

MQ
type: SiteQuality
SIO_000300: 5.965e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.79e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.92e-2

DP
type: SiteQuality
SIO_000300: 1.57214e5

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468152
ensembl transcript: ENST00000588028
gene symbol: ZBTB7C
hgvsc: ENST00000588028.1:c.-146+20754C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466944
ensembl transcript: ENST00000586047
gene symbol: ZBTB7C
hgvsc: ENST00000586047.1:c.-17+20754C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465832
ensembl transcript: ENST00000593159
gene symbol: ZBTB7C
hgvsc: ENST00000593159.1:c.-134C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467338
ensembl transcript: ENST00000589170
gene symbol: ZBTB7C
hgvsc: ENST00000589170.1:c.-66C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467877
ensembl transcript: ENST00000590800
gene symbol: ZBTB7C
hgvsc: ENST00000590800.1:c.-17+20754C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465265
ensembl transcript: ENST00000591279
gene symbol: ZBTB7C
hgvsc: ENST00000591279.1:c.-17+20754C>T
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 382
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1613
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3862
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 120
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 122
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 2170
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 5.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1947
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 39
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 190
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5000
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 86
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 220
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 137
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.313025210084034e-4
allele num: 7616
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3596
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.582e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.44e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.98e-2

QD
type: SiteQuality
SIO_000300: 9.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.663e0

DP
type: SiteQuality
SIO_000300: 1.57636e5

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465835
ensembl transcript: ENST00000592387
gene symbol: ZBTB7C
hgvsc: ENST00000592387.1:c.-119G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465494
ensembl transcript: ENST00000590374
gene symbol: ZBTB7C
hgvsc: ENST00000590374.1:c.-69G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468087
ensembl transcript: ENST00000592656
gene symbol: ZBTB7C
hgvsc: ENST00000592656.1:c.-119G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465265
ensembl transcript: ENST00000591279
gene symbol: ZBTB7C
hgvsc: ENST00000591279.1:c.-17+20751G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467147
ensembl transcript: ENST00000589077
gene symbol: ZBTB7C
hgvsc: ENST00000589077.1:c.-17+15204G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468537
ensembl transcript: ENST00000586525
gene symbol: ZBTB7C
hgvsc: ENST00000586525.1:c.-69G>C
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 382
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 121
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2174
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 120
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 3862
bin: 2.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1615
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 4
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 225
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 84
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1947
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5004
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 501
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 130
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3598
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.312680493567866e-4
allele num: 7618
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.57623e5

FS
type: SiteQuality
SIO_000300: 7.409e0

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-1

QD
type: SiteQuality
SIO_000300: 9.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.89e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.036e0

MQ
type: SiteQuality
SIO_000300: 5.934e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468254
ensembl transcript: ENST00000586438
gene symbol: ZBTB7C
hgvsc: ENST00000586438.1:c.-105G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467147
ensembl transcript: ENST00000589077
gene symbol: ZBTB7C
hgvsc: ENST00000589077.1:c.-17+15168G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000464724
ensembl transcript: ENST00000585404
gene symbol: ZBTB7C
hgvsc: ENST00000585404.1:c.-246+20715G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468306
ensembl transcript: ENST00000590855
gene symbol: ZBTB7C
hgvsc: ENST00000590855.1:c.-105G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465835
ensembl transcript: ENST00000592387
gene symbol: ZBTB7C
hgvsc: ENST00000592387.1:c.-155G>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468152
ensembl transcript: ENST00000588028
gene symbol: ZBTB7C
hgvsc: ENST00000588028.1:c.-146+20715G>C
variant of: http://identifiers.org/hgnc/31700

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

GenotypeDepth
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3822
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 132
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2192
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 382
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 4
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 121
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1625
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 190
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 39
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 101
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4979
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7610
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.785515320334262e-4
allele num: 3590
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.57555e5

VQSLOD
type: SiteQuality
SIO_000300: -1.676e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.02e-2

MQ
type: SiteQuality
SIO_000300: 5.933e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.28e0

FS
type: SiteQuality
SIO_000300: 1.184e0

MQRankSum
type: SiteQuality
SIO_000300: -2.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.246e0

QD
type: SiteQuality
SIO_000300: 7.59e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467147
ensembl transcript: ENST00000589077
gene symbol: ZBTB7C
hgvsc: ENST00000589077.1:c.-17+15160G>A
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468152
ensembl transcript: ENST00000588028
gene symbol: ZBTB7C
hgvsc: ENST00000588028.1:c.-146+20707G>A
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467456
ensembl transcript: ENST00000588566
gene symbol: ZBTB7C
hgvsc: ENST00000588566.1:c.-17+20707G>A
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468502
ensembl transcript: ENST00000588970
gene symbol: ZBTB7C
hgvsc: ENST00000588970.1:c.-168+20707G>A
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465265
ensembl transcript: ENST00000591279
gene symbol: ZBTB7C
hgvsc: ENST00000591279.1:c.-17+20707G>A
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467758
ensembl transcript: ENST00000591405
gene symbol: ZBTB7C
hgvsc: ENST00000591405.1:c.-17+20707G>A
variant of: http://identifiers.org/hgnc/31700

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

GenotypeDepth
all individuals: 122
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 4

GenotypeDepth
all individuals: 69
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 23
bin: 5.25e1
variant carriers: 3

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

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2226
bin: 2.5e0
variant carriers: 2

GenotypeDepth
all individuals: 150
bin: 7.5e0
variant carriers: 4

GenotypeDepth
all individuals: 3773
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1623
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 381
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 6.25e1
variant carriers: 3

GenotypeDepth
all individuals: 2
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4930
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2013
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 9.75e1
variant carriers: 15

GenotypeQuality
all individuals: 132
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 39
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3584
num of homozygotes: 0

African
type: Population
allele count: 15
allele frequency: 2.678571428571428e-2
allele num: 560
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.337e0

QD
type: SiteQuality
SIO_000300: 1.189e1

FS
type: SiteQuality
SIO_000300: 1.238e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.92e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.98e-1

DP
type: SiteQuality
SIO_000300: 1.5762e5

VQSLOD
type: SiteQuality
SIO_000300: 3.04e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468306
ensembl transcript: ENST00000590855
gene symbol: ZBTB7C
hgvsc: ENST00000590855.1:c.-143-40A>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467758
ensembl transcript: ENST00000591405
gene symbol: ZBTB7C
hgvsc: ENST00000591405.1:c.-17+20637A>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468814
ensembl transcript: ENST00000588149
gene symbol: ZBTB7C
hgvsc: ENST00000588149.1:c.-17+20027A>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000464724
ensembl transcript: ENST00000585404
gene symbol: ZBTB7C
hgvsc: ENST00000585404.1:c.-246+20637A>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465832
ensembl transcript: ENST00000593159
gene symbol: ZBTB7C
hgvsc: ENST00000593159.1:c.-207-44A>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465835
ensembl transcript: ENST00000592387
gene symbol: ZBTB7C
hgvsc: ENST00000592387.1:c.-193-40A>G
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 186
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2723
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1822
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 921
bin: 2.25e1
variant carriers: 3

GenotypeDepth
all individuals: 806
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1875
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 393
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 68
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 199
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 633
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2090
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 941
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 804
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1266
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 323
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 199
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 114
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3232
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.792114695340502e-3
allele num: 558
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 6.105006105006105e-4
allele num: 6552
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.13313e5

VQSLOD
type: SiteQuality
SIO_000300: -7.068e-1

QD
type: SiteQuality
SIO_000300: 1.381e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e0

MQRankSum
type: SiteQuality
SIO_000300: 1.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.12e-2

FS
type: SiteQuality
SIO_000300: 9.388e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.39e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468814
ensembl transcript: ENST00000588149
gene symbol: ZBTB7C
hgvsc: ENST00000588149.1:c.-17+20024C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467758
ensembl transcript: ENST00000591405
gene symbol: ZBTB7C
hgvsc: ENST00000591405.1:c.-17+20634C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467456
ensembl transcript: ENST00000588566
gene symbol: ZBTB7C
hgvsc: ENST00000588566.1:c.-17+20634C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467147
ensembl transcript: ENST00000589077
gene symbol: ZBTB7C
hgvsc: ENST00000589077.1:c.-17+15087C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000464724
ensembl transcript: ENST00000585404
gene symbol: ZBTB7C
hgvsc: ENST00000585404.1:c.-246+20634C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468087
ensembl transcript: ENST00000592656
gene symbol: ZBTB7C
hgvsc: ENST00000592656.1:c.-193-43C>T
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 2779
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 852
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1799
bin: 1.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 5
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 370
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1857
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 179
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 955
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 3
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 758
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 931
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 58
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 333
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 75
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1227
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2095
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 808
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3192
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 556
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.553277415346381e-4
allele num: 6438
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 112
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.13e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.19e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 6.5e0

DP
type: SiteQuality
SIO_000300: 1.1314e5

BaseQRankSum
type: SiteQuality
SIO_000300: -3.645e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.28e-2

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468019
ensembl transcript: ENST00000589194
gene symbol: ZBTB7C
hgvsc: ENST00000589194.1:c.-17+45G>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465832
ensembl transcript: ENST00000593159
gene symbol: ZBTB7C
hgvsc: ENST00000593159.1:c.-208+5649G>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468152
ensembl transcript: ENST00000588028
gene symbol: ZBTB7C
hgvsc: ENST00000588028.1:c.-146+5649G>T
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 3855
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 313
bin: 4.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 1018
bin: 2.25e1
variant carriers: 5

GenotypeDepth
all individuals: 261
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 753
bin: 3.75e1
variant carriers: 4

GenotypeDepth
all individuals: 409
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2008
bin: 2.75e1
variant carriers: 5

GenotypeDepth
all individuals: 7
bin: 6.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 125
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1506
bin: 3.25e1
variant carriers: 4

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 213
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3096
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 9.75e1
variant carriers: 20

GenotypeQuality
all individuals: 130
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2442
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 778
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 953
bin: 6.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 56
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3620
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

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

South Asian
type: Population
allele count: 21
allele frequency: 2.758801891749869e-3
allele num: 7612
num of homozygotes: 1

Other
type: Population
allele count: 1
allele frequency: 7.575757575757576e-3
allele num: 132
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.92929e5

QD
type: SiteQuality
SIO_000300: 1.251e1

MQ
type: SiteQuality
SIO_000300: 5.962e1

VQSLOD
type: SiteQuality
SIO_000300: 3.58e0

MQRankSum
type: SiteQuality
SIO_000300: 1.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.75e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.5e-2

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466006
ensembl transcript: ENST00000586743
gene symbol: ZBTB7C
hgvsc: ENST00000586743.1:c.-212+5634A>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468019
ensembl transcript: ENST00000589194
gene symbol: ZBTB7C
hgvsc: ENST00000589194.1:c.-17+30A>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465835
ensembl transcript: ENST00000592387
gene symbol: ZBTB7C
hgvsc: ENST00000592387.1:c.-194+5634A>C
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1168
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 261
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1518
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 3260
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 754
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2124
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 313
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 124
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2926
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2608
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 964
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 532
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.783964365256125e-4
allele num: 3592
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7618
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 562
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

DP
type: SiteQuality
SIO_000300: 1.92715e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.14e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.607e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.7e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.92e-1

QD
type: SiteQuality
SIO_000300: 1.286e1

MQ
type: SiteQuality
SIO_000300: 5.881e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468152
ensembl transcript: ENST00000588028
gene symbol: ZBTB7C
hgvsc: ENST00000588028.1:c.-146+5605G>A
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465832
ensembl transcript: ENST00000593159
gene symbol: ZBTB7C
hgvsc: ENST00000593159.1:c.-208+5605G>A
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466006
ensembl transcript: ENST00000586743
gene symbol: ZBTB7C
hgvsc: ENST00000586743.1:c.-212+5605G>A
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 202
bin: 7.5e0
variant carriers: 3

GenotypeDepth
all individuals: 752
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1167
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 124
bin: 4.75e1
variant carriers: 4

GenotypeDepth
all individuals: 24
bin: 5.75e1
variant carriers: 4

GenotypeDepth
all individuals: 2153
bin: 2.75e1
variant carriers: 2

GenotypeDepth
all individuals: 2855
bin: 2.5e0
variant carriers: 2

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

GenotypeDepth
all individuals: 315
bin: 4.25e1
variant carriers: 4

GenotypeDepth
all individuals: 22
bin: 1.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 41
bin: 5.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 7
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1528
bin: 3.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 962
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 142
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 9.75e1
variant carriers: 21

GenotypeQuality
all individuals: 27
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3005
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 369
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 322
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2524
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 529
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.063829787234043e-2
allele num: 188
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.783964365256125e-4
allele num: 3592
num of homozygotes: 0

African
type: Population
allele count: 17
allele frequency: 3.035714285714286e-2
allele num: 560
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.312680493567866e-4
allele num: 7618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.35e-1

DP
type: SiteQuality
SIO_000300: 1.92204e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.865e1

MQRankSum
type: SiteQuality
SIO_000300: 8.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 8.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.91e-2

QD
type: SiteQuality
SIO_000300: 1.176e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468752
ensembl transcript: ENST00000591526
gene symbol: ZBTB7C
hgvsc: ENST00000591526.1:c.-190+5595A>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468152
ensembl transcript: ENST00000588028
gene symbol: ZBTB7C
hgvsc: ENST00000588028.1:c.-146+5595A>C
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466006
ensembl transcript: ENST00000586743
gene symbol: ZBTB7C
hgvsc: ENST00000586743.1:c.-212+5595A>C
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 3
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2151
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 312
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 6.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1529
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 40
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2699
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1158
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 178
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 752
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 121
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2366
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 958
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3003
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 8.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3588
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.312680493567866e-4
allele num: 7618
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

FS
type: SiteQuality
SIO_000300: 1.133e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.066e0

MQRankSum
type: SiteQuality
SIO_000300: -4.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.59e-2

QD
type: SiteQuality
SIO_000300: 1.054e1

DP
type: SiteQuality
SIO_000300: 1.91021e5

VQSLOD
type: SiteQuality
SIO_000300: -1.504e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468537
ensembl transcript: ENST00000586525
gene symbol: ZBTB7C
hgvsc: ENST00000586525.1:c.-144+5570A>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466006
ensembl transcript: ENST00000586743
gene symbol: ZBTB7C
hgvsc: ENST00000586743.1:c.-212+5570A>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468152
ensembl transcript: ENST00000588028
gene symbol: ZBTB7C
hgvsc: ENST00000588028.1:c.-146+5570A>G
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 952
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2036
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 20
bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 312
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 169
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 161
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1519
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2654
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 120
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 212
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 750
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 40
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 143
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2105
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 914
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 547
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2663
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 226
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 519
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 556
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.313715186547556e-4
allele num: 7612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3578
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.838e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.64e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.422e0

DP
type: SiteQuality
SIO_000300: 1.87473e5

MQRankSum
type: SiteQuality
SIO_000300: 3.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.379999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.72e0

VQSLOD
type: SiteQuality
SIO_000300: -1.523e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465835
ensembl transcript: ENST00000592387
gene symbol: ZBTB7C
hgvsc: ENST00000592387.1:c.-194+5556C>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466088
ensembl transcript: ENST00000588053
gene symbol: ZBTB7C
hgvsc: ENST00000588053.1:c.-194+5556C>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468814
ensembl transcript: ENST00000588149
gene symbol: ZBTB7C
hgvsc: ENST00000588149.1:c.-17+4946C>G
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 6
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 722
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 40
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1374
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 961
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 120
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 654
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2904
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1724
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 211
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 309
bin: 4.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 3
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 177
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2075
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 814
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 222
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2243
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 663
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.31578947368421e-4
allele num: 7600
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3568
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.94e-2

QD
type: SiteQuality
SIO_000300: 1.025e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.06e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.485e0

MQ
type: SiteQuality
SIO_000300: 5.844e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.493e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.55e-1

DP
type: SiteQuality
SIO_000300: 1.82144e5

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468306
ensembl transcript: ENST00000590855
gene symbol: ZBTB7C
hgvsc: ENST00000590855.1:c.-144+645C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468019
ensembl transcript: ENST00000589194
gene symbol: ZBTB7C
hgvsc: ENST00000589194.1:c.-165+35C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466088
ensembl transcript: ENST00000588053
gene symbol: ZBTB7C
hgvsc: ENST00000588053.1:c.-194+645C>T
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1892
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 349
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 169
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1897
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 61
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 524
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1269
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 115
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3378
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 5.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 27
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 50
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 721
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2799
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1893
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1328
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2816
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4994
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 6.024096385542169e-3
allele num: 166
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 108
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.64e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.917e1

DP
type: SiteQuality
SIO_000300: 1.04888e5

MQRankSum
type: SiteQuality
SIO_000300: 8.159999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.36e-2

QD
type: SiteQuality
SIO_000300: 1.37e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

VQSLOD
type: SiteQuality
SIO_000300: -1.152e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465160
ensembl transcript: ENST00000590178
gene symbol: ZBTB7C
hgvsc: ENST00000590178.1:c.-144+641C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468019
ensembl transcript: ENST00000589194
gene symbol: ZBTB7C
hgvsc: ENST00000589194.1:c.-165+31C>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466088
ensembl transcript: ENST00000588053
gene symbol: ZBTB7C
hgvsc: ENST00000588053.1:c.-194+641C>T
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 61
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 419
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1836
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1623
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1704
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 171
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 1.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 116
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3261
bin: 2.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 14
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1820
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2785
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 62
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 200
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1915
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2850
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.946282600233554e-4
allele num: 5138
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 514
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 110
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.934e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.53e0

DP
type: SiteQuality
SIO_000300: 1.09576e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.122e1

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.15e-2

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466006
ensembl transcript: ENST00000586743
gene symbol: ZBTB7C
hgvsc: ENST00000586743.1:c.-212+587dupT
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468152
ensembl transcript: ENST00000588028
gene symbol: ZBTB7C
hgvsc: ENST00000588028.1:c.-146+587dupT
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465835
ensembl transcript: ENST00000592387
gene symbol: ZBTB7C
hgvsc: ENST00000592387.1:c.-194+587dupT
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 1283
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 576
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 184
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 61
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 115
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2445
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1270
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2025
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 701
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 7
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 211
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2118
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 61
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2396
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1904
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 540
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.688618709895306e-4
allele num: 5922
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 112
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3026
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.18582e5

BaseQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.87e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.532e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.46e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.41e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.2e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468537
ensembl transcript: ENST00000586525
gene symbol: ZBTB7C
hgvsc: ENST00000586525.1:c.-144+571A>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467877
ensembl transcript: ENST00000590800
gene symbol: ZBTB7C
hgvsc: ENST00000590800.1:c.-17+571A>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465760
ensembl transcript: ENST00000587107
gene symbol: ZBTB7C
hgvsc: ENST00000587107.1:c.-183A>G
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 14
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 480
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 164
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2403
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1670
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1305
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 983
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 115
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1416
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2048
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 135
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 818
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1925
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 112
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2968
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.730103806228374e-4
allele num: 5780
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.047e1

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

DP
type: SiteQuality
SIO_000300: 1.08479e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.23e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -5.874e-1

FS
type: SiteQuality
SIO_000300: 2.522e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465835
ensembl transcript: ENST00000592387
gene symbol: ZBTB7C
hgvsc: ENST00000592387.1:c.-194+568A>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467456
ensembl transcript: ENST00000588566
gene symbol: ZBTB7C
hgvsc: ENST00000588566.1:c.-17+568A>T
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467758
ensembl transcript: ENST00000591405
gene symbol: ZBTB7C
hgvsc: ENST00000591405.1:c.-17+568A>T
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 4
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1492
bin: 1.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1687
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1320
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 163
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2417
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 437
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 916
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 115
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 4.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1888
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2039
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2950
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.901140684410646e-3
allele num: 526
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 114
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.47e0

QD
type: SiteQuality
SIO_000300: 1.419e1

MQRankSum
type: SiteQuality
SIO_000300: -3.4e-2

DP
type: SiteQuality
SIO_000300: 1.07477e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.263e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.01e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.399e0

VQSLOD
type: SiteQuality
SIO_000300: -1.691e0

MQ
type: SiteQuality
SIO_000300: 5.895e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000464724
ensembl transcript: ENST00000585404
gene symbol: ZBTB7C
hgvsc: ENST00000585404.1:c.-246+565A>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000467456
ensembl transcript: ENST00000588566
gene symbol: ZBTB7C
hgvsc: ENST00000588566.1:c.-17+565A>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468152
ensembl transcript: ENST00000588028
gene symbol: ZBTB7C
hgvsc: ENST00000588028.1:c.-146+565A>G
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 128
bin: 3.75e1
variant carriers: 67

GenotypeDepth
all individuals: 61
bin: 4.25e1
variant carriers: 24

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 2

GenotypeDepth
all individuals: 1598
bin: 1.75e1
variant carriers: 819

GenotypeDepth
all individuals: 182
bin: 3.25e1
variant carriers: 89

GenotypeDepth
all individuals: 2070
bin: 2.5e0
variant carriers: 130

GenotypeDepth
all individuals: 1855
bin: 1.25e1
variant carriers: 757

GenotypeDepth
all individuals: 755
bin: 2.25e1
variant carriers: 448

GenotypeDepth
all individuals: 367
bin: 2.75e1
variant carriers: 202

GenotypeDepth
all individuals: 15
bin: 5.25e1
variant carriers: 5

GenotypeDepth
all individuals: 1309
bin: 7.5e0
variant carriers: 357

GenotypeDepth
all individuals: 1
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 33
bin: 4.75e1
variant carriers: 19

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

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 7
bin: 5.75e1
variant carriers: 5

GenotypeDepth
all individuals: 4
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 68
bin: 8.75e1
variant carriers: 50

GenotypeQuality
all individuals: 216
bin: 1.25e1
variant carriers: 34

GenotypeQuality
all individuals: 265
bin: 1.75e1
variant carriers: 50

GenotypeQuality
all individuals: 1009
bin: 2.25e1
variant carriers: 48

GenotypeQuality
all individuals: 1955
bin: 9.75e1
variant carriers: 1877

GenotypeQuality
all individuals: 194
bin: 4.25e1
variant carriers: 48

GenotypeQuality
all individuals: 95
bin: 7.25e1
variant carriers: 56

GenotypeQuality
all individuals: 508
bin: 3.25e1
variant carriers: 59

GenotypeQuality
all individuals: 383
bin: 2.75e1
variant carriers: 48

GenotypeQuality
all individuals: 154
bin: 5.25e1
variant carriers: 86

GenotypeQuality
all individuals: 80
bin: 5.75e1
variant carriers: 47

GenotypeQuality
all individuals: 1344
bin: 7.5e0
variant carriers: 74

GenotypeQuality
all individuals: 386
bin: 3.75e1
variant carriers: 65

GenotypeQuality
all individuals: 878
bin: 2.5e0
variant carriers: 5

GenotypeQuality
all individuals: 206
bin: 4.75e1
variant carriers: 76

GenotypeQuality
all individuals: 95
bin: 8.25e1
variant carriers: 67

GenotypeQuality
all individuals: 137
bin: 6.75e1
variant carriers: 85

GenotypeQuality
all individuals: 95
bin: 7.75e1
variant carriers: 64

GenotypeQuality
all individuals: 64
bin: 9.25e1
variant carriers: 38

GenotypeQuality
all individuals: 262
bin: 6.25e1
variant carriers: 51

East Asian
type: Population
allele count: 35
allele frequency: 1.842105263157895e-1
allele num: 190
num of homozygotes: 3

European (Non-Finnish)
type: Population
allele count: 845
allele frequency: 2.816666666666667e-1
allele num: 3000
num of homozygotes: 110

African
type: Population
allele count: 82
allele frequency: 1.541353383458647e-1
allele num: 532
num of homozygotes: 4

South Asian
type: Population
allele count: 1844
allele frequency: 3.168384879725086e-1
allele num: 5820
num of homozygotes: 307

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Latino
type: Population
allele count: 34
allele frequency: 1.931818181818182e-1
allele num: 176
num of homozygotes: 1

Other
type: Population
allele count: 18
allele frequency: 1.578947368421053e-1
allele num: 114
num of homozygotes: 2

DP
type: SiteQuality
SIO_000300: 1.07236e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.303e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.83e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.589e1

VQSLOD
type: SiteQuality
SIO_000300: 6.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.64e-2

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466006
ensembl transcript: ENST00000586743
gene symbol: ZBTB7C
hgvsc: ENST00000586743.1:c.-273-66256A>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000464724
ensembl transcript: ENST00000585404
gene symbol: ZBTB7C
hgvsc: ENST00000585404.1:c.-307-66256A>G
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 2198
bin: 2.5e0
variant carriers: 35

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

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

GenotypeDepth
all individuals: 3
bin: 1.25e1
variant carriers: 2

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

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

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 0
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 0
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 0
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 7.5e0
variant carriers: 20

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

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

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

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

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

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

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

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

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 6.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 49
bin: 1.25e1
variant carriers: 10

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

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

GenotypeQuality
all individuals: 43
bin: 2.25e1
variant carriers: 8

GenotypeQuality
all individuals: 45
bin: 1.75e1
variant carriers: 10

GenotypeQuality
all individuals: 734
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1444
bin: 7.5e0
variant carriers: 19

GenotypeQuality
all individuals: 2
bin: 6.25e1
variant carriers: 2

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

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

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

GenotypeQuality
all individuals: 1
bin: 7.25e1
variant carriers: 1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 5.0e-1
allele num: 2
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.75e-2

FS
type: SiteQuality
SIO_000300: 2.17e0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 5.503e3

QD
type: SiteQuality
SIO_000300: 1.903e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465760
ensembl transcript: ENST00000587107
gene symbol: ZBTB7C
hgvsc: ENST00000587107.1:c.-337-66337dupA
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466006
ensembl transcript: ENST00000586743
gene symbol: ZBTB7C
hgvsc: ENST00000586743.1:c.-273-66337dupA
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468306
ensembl transcript: ENST00000590855
gene symbol: ZBTB7C
hgvsc: ENST00000590855.1:c.-205-66337dupA
variant of: http://identifiers.org/hgnc/31700

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

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

GenotypeDepth
all individuals: 0
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2146
bin: 2.5e0
variant carriers: 2

GenotypeDepth
all individuals: 0
bin: 4.75e1
variant carriers: 0

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

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

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

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

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

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

GenotypeDepth
all individuals: 90
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 3.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 0
bin: 6.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

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

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

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

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

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

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

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

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 2.5e0
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 1938
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.25e1
variant carriers: 0

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

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

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.056e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

QD
type: SiteQuality
SIO_000300: 2.184e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.038e3

MQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465160
ensembl transcript: ENST00000590178
gene symbol: ZBTB7C
hgvsc: ENST00000590178.1:c.-205-66643A>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465760
ensembl transcript: ENST00000587107
gene symbol: ZBTB7C
hgvsc: ENST00000587107.1:c.-337-66643A>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465835
ensembl transcript: ENST00000592387
gene symbol: ZBTB7C
hgvsc: ENST00000592387.1:c.-255-66643A>G
variant of: http://identifiers.org/hgnc/31700

GenotypeDepth
all individuals: 13
bin: 1.25e1
variant carriers: 2

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

GenotypeDepth
all individuals: 301
bin: 7.5e0
variant carriers: 39

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

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

GenotypeDepth
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3456
bin: 2.5e0
variant carriers: 46

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

GenotypeDepth
all individuals: 0
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 0
bin: 6.75e1
variant carriers: 0

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

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

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

GenotypeDepth
all individuals: 0
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 8

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 9

GenotypeQuality
all individuals: 3061
bin: 7.5e0
variant carriers: 26

GenotypeQuality
all individuals: 178
bin: 2.25e1
variant carriers: 7

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

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

GenotypeQuality
all individuals: 1
bin: 7.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 407
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.75e1
variant carriers: 4

GenotypeQuality
all individuals: 8
bin: 6.25e1
variant carriers: 6

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

GenotypeQuality
all individuals: 45
bin: 1.75e1
variant carriers: 12

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

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

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

GenotypeQuality
all individuals: 2
bin: 8.25e1
variant carriers: 2

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

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

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 1

African
type: Population
allele count: 2
allele frequency: 1.25e-1
allele num: 16
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 5.0e-1
allele num: 2
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.225e0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

DP
type: SiteQuality
SIO_000300: 9.964e3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 1.669e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.57e-2

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465160
ensembl transcript: ENST00000590178
gene symbol: ZBTB7C
hgvsc: ENST00000590178.1:c.-205-66656G>A
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468019
ensembl transcript: ENST00000589194
gene symbol: ZBTB7C
hgvsc: ENST00000589194.1:c.-358-66656G>A
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468502
ensembl transcript: ENST00000588970
gene symbol: ZBTB7C
hgvsc: ENST00000588970.1:c.-229-66656G>A
variant of: http://identifiers.org/hgnc/31700

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

GenotypeDepth
all individuals: 3691
bin: 2.5e0
variant carriers: 11

GenotypeDepth
all individuals: 16
bin: 1.25e1
variant carriers: 3

GenotypeDepth
all individuals: 0
bin: 3.75e1
variant carriers: 0

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

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

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

GenotypeDepth
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 2.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 1
bin: 1.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 287
bin: 7.5e0
variant carriers: 13

GenotypeDepth
all individuals: 0
bin: 6.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 8
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 2

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

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 192
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 3346
bin: 7.5e0
variant carriers: 1

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

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

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 5

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

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 2

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

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

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

Other
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 1.363636363636364e-1
allele num: 22
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.83e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 1.383e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.27e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

DP
type: SiteQuality
SIO_000300: 1.0167e4

VQSLOD
type: SiteQuality
SIO_000300: 3.37e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000466088
ensembl transcript: ENST00000588053
gene symbol: ZBTB7C
hgvsc: ENST00000588053.1:c.-255-66706T>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000465832
ensembl transcript: ENST00000593159
gene symbol: ZBTB7C
hgvsc: ENST00000593159.1:c.-269-66706T>G
variant of: http://identifiers.org/hgnc/31700

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000184828
ensembl protein: ENSP00000468537
ensembl transcript: ENST00000586525
gene symbol: ZBTB7C
hgvsc: ENST00000586525.1:c.-205-66706T>G
variant of: http://identifiers.org/hgnc/31700

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

GenotypeDepth
all individuals: 0
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeDepth
all individuals: 23
bin: 1.25e1
variant carriers: 5

GenotypeDepth
all individuals: 0
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3534
bin: 2.5e0
variant carriers: 32

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

GenotypeDepth
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 338
bin: 7.5e0
variant carriers: 42

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

GenotypeDepth
all individuals: 2
bin: 2.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 0
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 405
bin: 2.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 207
bin: 2.25e1
variant carriers: 5

GenotypeQuality
all individuals: 3134
bin: 7.5e0
variant carriers: 17

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

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

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

GenotypeQuality
all individuals: 46
bin: 1.25e1
variant carriers: 12

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

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 56
bin: 1.75e1
variant carriers: 6

GenotypeQuality
all individuals: 8
bin: 6.75e1
variant carriers: 7

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

GenotypeQuality
all individuals: 4
bin: 7.25e1
variant carriers: 4

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

GenotypeQuality
all individuals: 10
bin: 6.25e1
variant carriers: 5

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

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.388888888888889e-1
allele num: 36
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.46e0

QD
type: SiteQuality
SIO_000300: 1.573e1

DP
type: SiteQuality
SIO_000300: 1.0439e4

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.42e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.86e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.46e-1

GenotypeQuality
all individuals: 5058
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 16964
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 108
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1446
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2380
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9626
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1010
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 124
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.493e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-2

DP
type: SiteQuality
SIO_000300: 4.07258e5

VQSLOD
type: SiteQuality
SIO_000300: 4.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1