7-27856089-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856089
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856089
    reference: chr 7
allele count: 1
allele frequency: 8.251642076773278e-6
allele num: 121188
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1339+76C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1810+76C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.547+76C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1810+76C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1886C>T
  hgvsp: ENSP00000379612.2:p.Ala629Val
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.1958C>T
  hgvsp: ENSP00000386515.1:p.Ala653Val
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1346+76C>T
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10654
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5278
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3234
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4126
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala629Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

7-27856096-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856096
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856096
    reference: chr 7
allele count: 1
allele frequency: 8.254775387561705e-6
allele num: 121142
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1346+83A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1893A>G
  hgvsp: ENST00000396319.2:c.1893A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.1965A>G
  hgvsp: ENST00000409980.1:c.1965A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.547+83A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1810+83A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1339+83A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1810+83A>G
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10638
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5267
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14271
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3057
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2223
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro631Pro
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

7-27856105-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856105
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856105
    reference: chr 7
allele count: 1
allele frequency: 8.264872638312644e-6
allele num: 120994
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1810+92A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1810+92A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1346+92A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1902A>G
  hgvsp: ENST00000396319.2:c.1902A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.1974A>G
  hgvsp: ENST00000409980.1:c.1974A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1339+92A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.547+92A>G
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14834
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21430
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14275
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7005
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gln634Gln
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

7-27856105-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856105
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856105
    reference: chr 7
allele count: 5
allele frequency: 4.132436319156322e-5
allele num: 120994
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.1974A>T
  hgvsp: ENSP00000386515.1:p.Gln658His
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1346+92A>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1902A>T
  hgvsp: ENSP00000379612.2:p.Gln634His
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.547+92A>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1810+92A>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1339+92A>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1810+92A>T
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14834
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4109
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3045
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4933
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gln634His
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP

7-27856119-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856119
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856119
    reference: chr 7
allele count: 11
allele frequency: 9.130297647703316e-5
allele num: 120478
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1346+106A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1916A>G
  hgvsp: ENSP00000379612.2:p.Tyr639Cys
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1810+106A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1810+106A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.1988A>G
  hgvsp: ENSP00000386515.1:p.Tyr663Cys
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.547+106A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1339+106A>G
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5233
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4907
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 764
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6907
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20980
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3018
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Tyr639Cys
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

7-27856126-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856126
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856126
    reference: chr 7
allele count: 1
allele frequency: 8.332361224523806e-6
allele num: 120014
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1339+113T>A
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1923T>A
  hgvsp: ENST00000396319.2:c.1923T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.547+113T>A
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.1995T>A
  hgvsp: ENST00000409980.1:c.1995T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1346+113T>A
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1810+113T>A
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1810+113T>A
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2947
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20243
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10247
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14307
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20518
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3220
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14266
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4083
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser641Ser
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

7-27856128-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856128
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856128
    reference: chr 7
allele count: 3
allele frequency: 2.50928435210278e-5
allele num: 119556
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.547+115A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.1997A>G
  hgvsp: ENSP00000386515.1:p.Gln666Arg
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1810+115A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1339+115A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1346+115A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1810+115A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1925A>G
  hgvsp: ENSP00000379612.2:p.Gln642Arg
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13987
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10065
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2945
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20175
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6668
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3220
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4079
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14268
  bin: 9.75e1
  variant carriers: 3
hgvs: p.Gln642Arg
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/7-27856134-CAA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856134
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856132
    reference: chr 7
allele count: 10
allele frequency: 8.385041086701326e-5
allele num: 119260
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1810+122_1810+123delAA
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1932_1933delAA
  hgvsp: ENSP00000379612.2:p.Asp646TrpfsTer10
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2004_2005delAA
  hgvsp: ENSP00000386515.1:p.Asp670TrpfsTer10
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1346+122_*1346+123delAA
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1810+122_1810+123delAA
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1339+122_1339+123delAA
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.547+122_547+123delAA
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13752
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 20122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9933
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2943
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6605
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14272
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 4843
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1975
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp646TrpfsTer10
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: CAA
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

7-27856148-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856148
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856148
    reference: chr 7
allele count: 2
allele frequency: 1.694053870913095e-5
allele num: 118060
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1346+135A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1936+9A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2008+9A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.547+135A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1810+135A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1339+135A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1810+135A>G
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5150
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12518
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2508
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9568
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19740
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2908
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14271
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4824
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4067
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

7-27856152-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856152
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856152
    reference: chr 7
allele count: 1
allele frequency: 8.493434575073469e-6
allele num: 117738
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.547+139T>A
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1936+13T>A
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1810+139T>A
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1339+139T>A
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2008+13T>A
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1346+139T>A
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1810+139T>A
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9527
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2754
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19581
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17697
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4821
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2904
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6307
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4066
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-27856181-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856181
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856180
    reference: chr 7
allele count: 4
allele frequency: 3.496381245410999e-5
allele num: 114404
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1936+43delA
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1810+169delA
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1810+169delA
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1339+169delA
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1346+169delA
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2008+43delA
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.547+169delA
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11278
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3001
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18370
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9248
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4056
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3216
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2862
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 902
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14271
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 932
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: GA
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

7-27856182-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856182
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856183
    reference: chr 7
allele count: 1
allele frequency: 8.757180888328429e-6
allele num: 114192
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1339+176dupT
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1346+176dupT
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1810+176dupT
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1810+176dupT
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2008+50dupT
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1936+50dupT
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.547+176dupT
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9239
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11255
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2903
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2861
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 925
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4773
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 782
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-27856184-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856184
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856184
    reference: chr 7
allele count: 2
allele frequency: 1.762331917593359e-5
allele num: 113486
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.547+171T>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1339+171T>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1810+171T>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1936+45T>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1346+171T>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1810+171T>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2008+45T>G
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11276
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5034
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3060
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 752
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5902
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2846
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 949
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2599
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2200
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 644
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 995
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14274
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 1
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

7-27856186-T-TCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856186
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856188
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 113640
alternate allele: TCC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1339+173_1339+174insCC
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2008+47_2008+48insCC
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1810+173_1810+174insCC
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1810+173_1810+174insCC
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1936+47_1936+48insCC
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.547+173_547+174insCC
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1346+173_*1346+174insCC
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 3070
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9205
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4055
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4766
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2728
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 647
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 951
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 890
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/7-27856190-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856190
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856190
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 113016
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2008+51A>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.547+177A>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1810+177A>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1810+177A>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1339+177A>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1936+51A>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1346+177A>C
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3159
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9304
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3216
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1301
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4055
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2200
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14274
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 934
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2846
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

7-27856460-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856460
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856459
    reference: chr 7
allele count: 1
allele frequency: 8.358967500334358e-6
allele num: 119632
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1347-48delA
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1340-48delA
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2009-48delA
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1937-48delA
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1811-48delA
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.548-48delA
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1811-48delA
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11325
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4073
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7648
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13716
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4563
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1753
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 786
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6138
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11254
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1845
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4815
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: TA
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

7-27856467-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856467
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856467
    reference: chr 7
allele count: 2
allele frequency: 1.671821449469197e-5
allele num: 119630
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1811-42A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.548-42A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1340-42A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1811-42A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1937-42A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2009-42A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1347-42A>G
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13872
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10084
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11563
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1073
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 859
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3117
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6218
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13600
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16549
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum

7-27856467-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856467
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856467
    reference: chr 7
allele count: 9
allele frequency: 7.523196522611385e-5
allele num: 119630
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1340-42A>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1937-42A>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2009-42A>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.548-42A>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1347-42A>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1811-42A>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1811-42A>T
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13872
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11563
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10084
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13600
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6218
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 606
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3565
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1117
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

7-27856480-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856480
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856480
    reference: chr 7
allele count: 1
allele frequency: 8.349893956346754e-6
allele num: 119762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1340-29A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1937-29A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2009-29A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.548-29A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1811-29A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1347-29A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1811-29A>G
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7729
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11976
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11179
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16571
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3197
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4971
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 834
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6368
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2412
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum

7-27856481-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856481
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856481
    reference: chr 7
allele count: 1
allele frequency: 8.34752412434472e-6
allele num: 119796
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1347-28C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1340-28C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1811-28C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.548-28C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2009-28C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1937-28C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1811-28C>T
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7732
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11225
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2503
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14528
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12004
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2418
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4990
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP

7-27856487-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856487
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856487
    reference: chr 7
allele count: 1
allele frequency: 8.341675008341675e-6
allele num: 119880
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2009-22C>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1811-22C>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.548-22C>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1347-22C>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1340-22C>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1811-22C>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1937-22C>G
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12115
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2506
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7752
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11551
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16112
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5030
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6471
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

7-27856498-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856498
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856498
    reference: chr 7
allele count: 1
allele frequency: 8.328058896032513e-6
allele num: 120076
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2009-11T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1937-11T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1811-11T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1340-11T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.548-11T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1811-11T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1347-11T>C
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7794
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6537
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5075
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2466
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3273
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 4.25e1
  variant carriers: 0
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: T
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/7-27856502-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856502
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856502
    reference: chr 7
allele count: 2
allele frequency: 1.664946222237022e-5
allele num: 120124
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.548-7A>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2009-7A>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1937-7A>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1811-7A>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1811-7A>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1347-7A>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1340-7A>C
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14905
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3286
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
hgvs: c.1937-7A>C
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ

7-27856514-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856514
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856514
    reference: chr 7
allele count: 1
allele frequency: 8.304544246611745e-6
allele num: 120416
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1942G>C
  hgvsp: ENSP00000379612.2:p.Ala648Pro
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.553G>C
  hgvsp: ENSP00000412575.2:p.Ala185Pro
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1352G>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2014G>C
  hgvsp: ENSP00000386515.1:p.Ala672Pro
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1345G>C
  hgvsp: ENSP00000391907.2:p.Ala449Pro
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1816G>C
  hgvsp: ENSP00000444811.1:p.Ala606Pro
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1816G>C
  hgvsp: ENSP00000265393.6:p.Ala606Pro
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12422
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4609
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2515
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6618
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4720
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2476
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala648Pro
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/7-27856515-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856515
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856515
    reference: chr 7
allele count: 1
allele frequency: 8.303440945927993e-6
allele num: 120432
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2015C>A
  hgvsp: ENSP00000386515.1:p.Ala672Glu
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1817C>A
  hgvsp: ENSP00000265393.6:p.Ala606Glu
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1943C>A
  hgvsp: ENSP00000379612.2:p.Ala648Glu
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1346C>A
  hgvsp: ENSP00000391907.2:p.Ala449Glu
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1353C>A
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1817C>A
  hgvsp: ENSP00000444811.1:p.Ala606Glu
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.554C>A
  hgvsp: ENSP00000412575.2:p.Ala185Glu
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4608
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7814
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15135
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12424
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16609
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5133
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4720
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6619
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala648Glu
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

7-27856515-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856515
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856515
    reference: chr 7
allele count: 1
allele frequency: 8.303440945927993e-6
allele num: 120432
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2015C>G
  hgvsp: ENSP00000386515.1:p.Ala672Gly
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1817C>G
  hgvsp: ENSP00000265393.6:p.Ala606Gly
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1353C>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.554C>G
  hgvsp: ENSP00000412575.2:p.Ala185Gly
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1817C>G
  hgvsp: ENSP00000444811.1:p.Ala606Gly
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1346C>G
  hgvsp: ENSP00000391907.2:p.Ala449Gly
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1943C>G
  hgvsp: ENSP00000379612.2:p.Ala648Gly
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15135
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4608
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7814
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12424
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11822
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16895
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5133
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3311
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3674
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala648Gly
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/7-27856516-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856516
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856516
    reference: chr 7
allele count: 1
allele frequency: 8.299995020002988e-6
allele num: 120482
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1347A>C
  hgvsp: ENST00000433216.2:c.1347A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1944A>C
  hgvsp: ENST00000396319.2:c.1944A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1818A>C
  hgvsp: ENST00000265393.6:c.1818A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1354A>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1818A>C
  hgvsp: ENST00000543117.1:c.1818A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.555A>C
  hgvsp: ENST00000457186.2:c.555A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2016A>C
  hgvsp: ENST00000409980.1:c.2016A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 11849
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4609
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7814
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15152
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3315
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala648Ala
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

7-27856520-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856520
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856520
    reference: chr 7
allele count: 1
allele frequency: 8.294074713025015e-6
allele num: 120568
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1948G>A
  hgvsp: ENSP00000379612.2:p.Gly650Ser
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1822G>A
  hgvsp: ENSP00000444811.1:p.Gly608Ser
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1351G>A
  hgvsp: ENSP00000391907.2:p.Gly451Ser
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.559G>A
  hgvsp: ENSP00000412575.2:p.Gly187Ser
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1358G>A
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1822G>A
  hgvsp: ENSP00000265393.6:p.Gly608Ser
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2020G>A
  hgvsp: ENSP00000386515.1:p.Gly674Ser
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11852
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7817
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4610
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15196
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16612
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16984
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3321
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly650Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ

7-27856523-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856523
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856523
    reference: chr 7
allele count: 1
allele frequency: 8.291598951941893e-6
allele num: 120604
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2023G>A
  hgvsp: ENSP00000386515.1:p.Ala675Thr
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1951G>A
  hgvsp: ENSP00000379612.2:p.Ala651Thr
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1825G>A
  hgvsp: ENSP00000444811.1:p.Ala609Thr
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1354G>A
  hgvsp: ENSP00000391907.2:p.Ala452Thr
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1361G>A
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.562G>A
  hgvsp: ENSP00000412575.2:p.Ala188Thr
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1825G>A
  hgvsp: ENSP00000265393.6:p.Ala609Thr
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11856
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7821
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4611
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2515
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16615
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5133
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16982
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3672
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala651Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

7-27856524-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856524
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856524
    reference: chr 7
allele count: 1
allele frequency: 8.290774026663129e-6
allele num: 120616
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1952C>T
  hgvsp: ENSP00000379612.2:p.Ala651Val
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1355C>T
  hgvsp: ENSP00000391907.2:p.Ala452Val
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1362C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2024C>T
  hgvsp: ENSP00000386515.1:p.Ala675Val
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.563C>T
  hgvsp: ENSP00000412575.2:p.Ala188Val
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1826C>T
  hgvsp: ENSP00000444811.1:p.Ala609Val
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1826C>T
  hgvsp: ENSP00000265393.6:p.Ala609Val
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11847
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2519
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4611
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4724
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6661
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala651Val
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

7-27856537-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856537
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856537
    reference: chr 7
allele count: 5
allele frequency: 4.14119829713926e-5
allele num: 120738
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1839T>C
  hgvsp: ENST00000543117.1:c.1839T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.576T>C
  hgvsp: ENST00000457186.2:c.576T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2037T>C
  hgvsp: ENST00000409980.1:c.2037T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1375T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1368T>C
  hgvsp: ENST00000433216.2:c.1368T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1965T>C
  hgvsp: ENST00000396319.2:c.1965T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1839T>C
  hgvsp: ENST00000265393.6:c.1839T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7825
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15254
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2520
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3675
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3336
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2476
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17041
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp655Asp
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

7-27856540-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856540
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856540
    reference: chr 7
allele count: 1
allele frequency: 8.279242283746192e-6
allele num: 120784
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1378A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1842A>G
  hgvsp: ENST00000543117.1:c.1842A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.579A>G
  hgvsp: ENST00000457186.2:c.579A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1842A>G
  hgvsp: ENST00000265393.6:c.1842A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1371A>G
  hgvsp: ENST00000433216.2:c.1371A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2040A>G
  hgvsp: ENST00000409980.1:c.2040A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1968A>G
  hgvsp: ENST00000396319.2:c.1968A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7827
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11882
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15259
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6673
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16624
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17056
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5137
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Glu656Glu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

7-27856552-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856552
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856552
    reference: chr 7
allele count: 3
allele frequency: 2.481512730160306e-5
allele num: 120894
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2052A>G
  hgvsp: ENST00000409980.1:c.2052A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.1980A>G
  hgvsp: ENST00000396319.2:c.1980A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1383A>G
  hgvsp: ENST00000433216.2:c.1383A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1854A>G
  hgvsp: ENST00000543117.1:c.1854A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.591A>G
  hgvsp: ENST00000457186.2:c.591A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1854A>G
  hgvsp: ENST00000265393.6:c.1854A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1390A>G
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7829
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12494
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6679
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17153
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16623
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3677
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro660Pro
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-27856575-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856575
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856575
    reference: chr 7
allele count: 3
allele frequency: 2.476677949310658e-5
allele num: 121130
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1877G>T
  hgvsp: ENSP00000265393.6:p.Gly626Val
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1413G>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.614G>T
  hgvsp: ENSP00000412575.2:p.Gly205Val
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2075G>T
  hgvsp: ENSP00000386515.1:p.Gly692Val
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1877G>T
  hgvsp: ENSP00000444811.1:p.Gly626Val
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1406G>T
  hgvsp: ENSP00000391907.2:p.Gly469Val
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2003G>T
  hgvsp: ENSP00000379612.2:p.Gly668Val
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7829
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16628
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4735
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5152
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2484
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly668Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD

7-27856580-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856580
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856580
    reference: chr 7
allele count: 1
allele frequency: 8.253549026081216e-6
allele num: 121160
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2080G>A
  hgvsp: ENSP00000386515.1:p.Glu694Lys
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2008G>A
  hgvsp: ENSP00000379612.2:p.Glu670Lys
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.619G>A
  hgvsp: ENSP00000412575.2:p.Glu207Lys
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1411G>A
  hgvsp: ENSP00000391907.2:p.Glu471Lys
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1882G>A
  hgvsp: ENSP00000265393.6:p.Glu628Lys
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1882G>A
  hgvsp: ENSP00000444811.1:p.Glu628Lys
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1418G>A
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12173
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7832
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17525
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3348
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6730
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu670Lys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

7-27856584-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856584
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856584
    reference: chr 7
allele count: 1
allele frequency: 8.252595441266279e-6
allele num: 121174
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1415A>T
  hgvsp: ENSP00000391907.2:p.Asp472Val
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1886A>T
  hgvsp: ENSP00000265393.6:p.Asp629Val
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.623A>T
  hgvsp: ENSP00000412575.2:p.Asp208Val
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2012A>T
  hgvsp: ENSP00000379612.2:p.Asp671Val
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1886A>T
  hgvsp: ENSP00000444811.1:p.Asp629Val
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2084A>T
  hgvsp: ENSP00000386515.1:p.Asp695Val
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1422A>T
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12525
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12185
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4736
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16629
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6727
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5155
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp671Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum

7-27856587-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856587
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856587
    reference: chr 7
allele count: 1
allele frequency: 8.251778258214646e-6
allele num: 121186
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.626A>G
  hgvsp: ENSP00000412575.2:p.Asn209Ser
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1889A>G
  hgvsp: ENSP00000265393.6:p.Asn630Ser
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1425A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1418A>G
  hgvsp: ENSP00000391907.2:p.Asn473Ser
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1889A>G
  hgvsp: ENSP00000444811.1:p.Asn630Ser
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2015A>G
  hgvsp: ENSP00000379612.2:p.Asn672Ser
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2087A>G
  hgvsp: ENSP00000386515.1:p.Asn696Ser
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12188
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12527
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3680
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5157
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4736
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asn672Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

7-27856588-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856588
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856588
    reference: chr 7
allele count: 2
allele frequency: 1.650355651642929e-5
allele num: 121186
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2088T>C
  hgvsp: ENST00000409980.1:c.2088T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.627T>C
  hgvsp: ENST00000457186.2:c.627T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1890T>C
  hgvsp: ENST00000543117.1:c.1890T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1419T>C
  hgvsp: ENST00000433216.2:c.1419T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1890T>C
  hgvsp: ENST00000265393.6:c.1890T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2016T>C
  hgvsp: ENST00000396319.2:c.2016T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1426T>C
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12527
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15483
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4737
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6734
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3680
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3353
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asn672Asn
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

7-27856594-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856594
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856594
    reference: chr 7
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2094C>T
  hgvsp: ENST00000409980.1:c.2094C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2022C>T
  hgvsp: ENST00000396319.2:c.2022C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1896C>T
  hgvsp: ENST00000265393.6:c.1896C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1432C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.633C>T
  hgvsp: ENST00000457186.2:c.633C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1896C>T
  hgvsp: ENST00000543117.1:c.1896C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1425C>T
  hgvsp: ENST00000433216.2:c.1425C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7829
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12197
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4737
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16629
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6740
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val674Val
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

7-27856597-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856597
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856597
    reference: chr 7
allele count: 1
allele frequency: 8.249463784853985e-6
allele num: 121220
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1428C>T
  hgvsp: ENST00000433216.2:c.1428C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.636C>T
  hgvsp: ENST00000457186.2:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1899C>T
  hgvsp: ENST00000265393.6:c.1899C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2097C>T
  hgvsp: ENST00000409980.1:c.2097C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2025C>T
  hgvsp: ENST00000396319.2:c.2025C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1435C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1899C>T
  hgvsp: ENST00000543117.1:c.1899C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7832
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12532
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16629
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6740
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3350
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Cys675Cys
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

7-27856600-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856600
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856600
    reference: chr 7
allele count: 1
allele frequency: 8.249327679794096e-6
allele num: 121222
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1431C>G
  hgvsp: ENSP00000391907.2:p.Ser477Arg
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2028C>G
  hgvsp: ENSP00000379612.2:p.Ser676Arg
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1902C>G
  hgvsp: ENSP00000265393.6:p.Ser634Arg
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.639C>G
  hgvsp: ENSP00000412575.2:p.Ser213Arg
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1438C>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2100C>G
  hgvsp: ENSP00000386515.1:p.Ser700Arg
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1902C>G
  hgvsp: ENSP00000444811.1:p.Ser634Arg
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12201
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7829
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12534
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16629
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4736
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3352
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17618
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser676Arg
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

7-27856611-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856611
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856611
    reference: chr 7
allele count: 1
allele frequency: 8.248102936324645e-6
allele num: 121240
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1913G>C
  hgvsp: ENSP00000265393.6:p.Arg638Pro
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1913G>C
  hgvsp: ENSP00000444811.1:p.Arg638Pro
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2039G>C
  hgvsp: ENSP00000379612.2:p.Arg680Pro
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.650G>C
  hgvsp: ENSP00000412575.2:p.Arg217Pro
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1442G>C
  hgvsp: ENSP00000391907.2:p.Arg481Pro
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1449G>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2111G>C
  hgvsp: ENSP00000386515.1:p.Arg704Pro
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7828
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12541
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5152
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6738
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3680
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg680Pro
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

7-27856612-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856612
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856612
    reference: chr 7
allele count: 1
allele frequency: 8.248239000973292e-6
allele num: 121238
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1914A>G
  hgvsp: ENST00000265393.6:c.1914A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.651A>G
  hgvsp: ENST00000457186.2:c.651A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1443A>G
  hgvsp: ENST00000433216.2:c.1443A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2112A>G
  hgvsp: ENST00000409980.1:c.2112A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1914A>G
  hgvsp: ENST00000543117.1:c.1914A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2040A>G
  hgvsp: ENST00000396319.2:c.2040A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1450A>G
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7827
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12235
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12543
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17692
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4740
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2488
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg680Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

7-27856618-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856618
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856618
    reference: chr 7
allele count: 1
allele frequency: 8.24783082049421e-6
allele num: 121244
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1456T>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1449T>G
  hgvsp: ENSP00000391907.2:p.Phe483Leu
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1920T>G
  hgvsp: ENSP00000444811.1:p.Phe640Leu
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2118T>G
  hgvsp: ENSP00000386515.1:p.Phe706Leu
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1920T>G
  hgvsp: ENSP00000265393.6:p.Phe640Leu
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2046T>G
  hgvsp: ENSP00000379612.2:p.Phe682Leu
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.657T>G
  hgvsp: ENSP00000412575.2:p.Phe219Leu
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12227
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3680
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2487
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Phe682Leu
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

7-27856623-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856623
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856623
    reference: chr 7
allele count: 1
allele frequency: 8.248239000973292e-6
allele num: 121238
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2123G>A
  hgvsp: ENSP00000386515.1:p.Arg708Gln
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1461G>A
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.662G>A
  hgvsp: ENSP00000412575.2:p.Arg221Gln
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1925G>A
  hgvsp: ENSP00000265393.6:p.Arg642Gln
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1925G>A
  hgvsp: ENSP00000444811.1:p.Arg642Gln
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2051G>A
  hgvsp: ENSP00000379612.2:p.Arg684Gln
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1454G>A
  hgvsp: ENSP00000391907.2:p.Arg485Gln
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12227
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12538
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7827
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15526
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3680
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17686
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg684Gln
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff

7-27856632-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856632
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856632
    reference: chr 7
allele count: 1
allele frequency: 8.247966876165026e-6
allele num: 121242
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2132G>T
  hgvsp: ENSP00000386515.1:p.Gly711Val
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1463G>T
  hgvsp: ENSP00000391907.2:p.Gly488Val
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.671G>T
  hgvsp: ENSP00000412575.2:p.Gly224Val
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1470G>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1934G>T
  hgvsp: ENSP00000265393.6:p.Gly645Val
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1934G>T
  hgvsp: ENSP00000444811.1:p.Gly645Val
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2060G>T
  hgvsp: ENSP00000379612.2:p.Gly687Val
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12226
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15533
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12537
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7825
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2487
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4738
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly687Val
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD

7-27856657-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856657
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856657
    reference: chr 7
allele count: 2
allele frequency: 1.653220473482343e-5
allele num: 120976
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1488A>G
  hgvsp: ENST00000433216.2:c.1488A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2085A>G
  hgvsp: ENST00000396319.2:c.2085A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2157A>G
  hgvsp: ENST00000409980.1:c.2157A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1959A>G
  hgvsp: ENST00000265393.6:c.1959A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1959A>G
  hgvsp: ENST00000543117.1:c.1959A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1495A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.696A>G
  hgvsp: ENST00000457186.2:c.696A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6645
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5130
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 2.25e1
  variant carriers: 0
hgvs: c.2085A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/7-27856660-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856660
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856660
    reference: chr 7
allele count: 1
allele frequency: 8.268289456277286e-6
allele num: 120944
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.696+3A>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1488+3A>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1959+3A>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1959+3A>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2085+3A>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1495+3A>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2157+3A>C
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7786
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4722
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6634
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: c.2085+3A>C
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

7-27856663-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856663
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856663
    reference: chr 7
allele count: 1
allele frequency: 8.271845945141119e-6
allele num: 120892
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1488+6T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2157+6T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1959+6T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2085+6T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.696+6T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1959+6T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1495+6T>C
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7785
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12375
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6622
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2481
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16620
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3675
  bin: 9.25e1
  variant carriers: 0
hgvs: c.2085+6T>C
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

7-27856680-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856680
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856680
    reference: chr 7
allele count: 1
allele frequency: 8.302613662781043e-6
allele num: 120444
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1959+23G>A
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2157+23G>A
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1495+23G>A
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.696+23G>A
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2085+23G>A
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1488+23G>A
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1959+23G>A
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11727
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11850
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7714
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15726
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3670
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2475
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5076
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum

7-27856689-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856689
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856689
    reference: chr 7
allele count: 1
allele frequency: 8.324038157390913e-6
allele num: 120134
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2085+32C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1495+32C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2157+32C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1488+32C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.696+32C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1959+32C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1959+32C>T
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11496
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11293
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3222
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1894
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14308
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

7-27856696-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856696
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856696
    reference: chr 7
allele count: 1
allele frequency: 8.339866228545694e-6
allele num: 119906
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1495+39T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2085+39T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1488+39T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2157+39T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.696+39T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1959+39T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1959+39T>C
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2242
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10912
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 810
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2470
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3169
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5805
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16616
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

7-27856697-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856697
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856697
    reference: chr 7
allele count: 7
allele frequency: 5.845023380093521e-5
allele num: 119760
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1959+40A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1488+40A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2085+40A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2157+40A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1495+40A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1959+40A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.696+40A>G
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2773
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2520
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11198
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12757
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10849
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7661
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1280
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 813
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5789
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3668
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

7-27856704-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27856704
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27856704
    reference: chr 7
allele count: 1
allele frequency: 8.39545973537511e-6
allele num: 119112
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1959+47A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2157+47A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1959+47A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1488+47A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2085+47A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.696+47A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1495+47A>G
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4575
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11244
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11011
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2519
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3667
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4692
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1261
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11268
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 818
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1628
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum

7-27867307-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27867307
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27867307
    reference: chr 7
allele count: 3
allele frequency: 2.489626556016598e-5
allele num: 120500
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1489-50T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.697-50T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2086-50T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1960-50T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1496-50T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2158-50T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1960-50T>C
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2347
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6984
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6444
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4517
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1035
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1452
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2871
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2678
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1643
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

7-27867315-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27867315
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27867315
    reference: chr 7
allele count: 1
allele frequency: 8.296964970213896e-6
allele num: 120526
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1489-42G>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1960-42G>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1496-42G>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2086-42G>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.697-42G>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1960-42G>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2158-42G>T
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7228
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4925
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6986
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4520
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36990
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1644
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2934
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

7-27867320-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27867320
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27867320
    reference: chr 7
allele count: 100
allele frequency: 8.294212298657997e-4
allele num: 120566
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1960-37A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2158-37A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.697-37A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2086-37A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1960-37A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1489-37A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1496-37A>G
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5973
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7226
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6985
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4526
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5872
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5185
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6461
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2974
  bin: 9.75e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 1456
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7074
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2695
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD

7-27867325-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27867325
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27867325
    reference: chr 7
allele count: 2
allele frequency: 1.657275439177991e-5
allele num: 120680
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1489-32T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1960-32T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1960-32T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2086-32T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1496-32T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2158-32T>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.697-32T>C
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6002
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2965
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6474
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6991
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4525
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2714
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2997
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7601
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

7-27867336-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27867336
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27867336
    reference: chr 7
allele count: 1
allele frequency: 8.268426187759421e-6
allele num: 120942
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1960-21C>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1496-21C>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1960-21C>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2158-21C>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1489-21C>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2086-21C>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.697-21C>G
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6481
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6990
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6079
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1472
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37006
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

7-27867336-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27867336
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27867336
    reference: chr 7
allele count: 1
allele frequency: 8.268426187759421e-6
allele num: 120942
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.697-21C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1960-21C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1496-21C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2086-21C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1960-21C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1489-21C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2158-21C>T
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6990
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6481
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6079
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7226
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1652
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1472
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2787
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

7-27867350-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27867350
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27867350
    reference: chr 7
allele count: 1
allele frequency: 8.252731654177533e-6
allele num: 121172
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1496-7C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1960-7C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1489-7C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1960-7C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2086-7C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.697-7C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2158-7C>T
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6107
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5661
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6994
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7230
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5880
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1647
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2788
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2730
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37007
  bin: 9.75e1
  variant carriers: 1
hgvs: c.2086-7C>T
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

7-27867352-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27867352
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27867352
    reference: chr 7
allele count: 12
allele frequency: 9.90033661144479e-5
allele num: 121208
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1960-5C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1489-5C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2086-5C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2158-5C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1960-5C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.697-5C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1496-5C>T
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6102
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6487
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5879
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6990
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5691
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2974
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7224
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1484
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2731
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: c.2086-5C>T
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD

7-27867364-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27867364
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27867364
    reference: chr 7
allele count: 110
allele frequency: 9.067528356634134e-4
allele num: 121312
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1967A>G
  hgvsp: ENSP00000444811.1:p.Glu656Gly
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1503A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.704A>G
  hgvsp: ENSP00000412575.2:p.Glu235Gly
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2093A>G
  hgvsp: ENSP00000379612.2:p.Glu698Gly
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2165A>G
  hgvsp: ENSP00000386515.1:p.Glu722Gly
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1967A>G
  hgvsp: ENSP00000265393.6:p.Glu656Gly
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1496A>G
  hgvsp: ENSP00000391907.2:p.Glu499Gly
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5879
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6473
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5704
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4531
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6992
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 7.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 6411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7214
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 9.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1479
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2718
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Glu698Gly
num of homozygotes: 3
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

7-27867373-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27867373
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27867373
    reference: chr 7
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1505C>T
  hgvsp: ENSP00000391907.2:p.Pro502Leu
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1976C>T
  hgvsp: ENSP00000265393.6:p.Pro659Leu
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1976C>T
  hgvsp: ENSP00000444811.1:p.Pro659Leu
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2102C>T
  hgvsp: ENSP00000379612.2:p.Pro701Leu
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.713C>T
  hgvsp: ENSP00000412575.2:p.Pro238Leu
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1512C>T
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2174C>T
  hgvsp: ENSP00000386515.1:p.Pro725Leu
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7229
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5881
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5736
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6126
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6992
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6412
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6483
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1492
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3177
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3005
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro701Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum

7-27867375-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27867375
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27867375
    reference: chr 7
allele count: 21
allele frequency: 1.730816780680788e-4
allele num: 121330
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1978A>G
  hgvsp: ENSP00000265393.6:p.Thr660Ala
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1514A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1507A>G
  hgvsp: ENSP00000391907.2:p.Thr503Ala
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.715A>G
  hgvsp: ENSP00000412575.2:p.Thr239Ala
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2104A>G
  hgvsp: ENSP00000379612.2:p.Thr702Ala
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1978A>G
  hgvsp: ENSP00000444811.1:p.Thr660Ala
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2176A>G
  hgvsp: ENSP00000386515.1:p.Thr726Ala
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6990
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5879
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6480
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4531
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5735
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7226
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3176
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr702Ala
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: A
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

7-27867381-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27867381
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27867381
    reference: chr 7
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1984C>T
  hgvsp: ENSP00000444811.1:p.Pro662Ser
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.721C>T
  hgvsp: ENSP00000412575.2:p.Pro241Ser
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2110C>T
  hgvsp: ENSP00000379612.2:p.Pro704Ser
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1513C>T
  hgvsp: ENSP00000391907.2:p.Pro505Ser
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1984C>T
  hgvsp: ENSP00000265393.6:p.Pro662Ser
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2182C>T
  hgvsp: ENSP00000386515.1:p.Pro728Ser
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1520C>T
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7229
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6993
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6481
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5741
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5881
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2727
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3177
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37000
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro704Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/7-27867392-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27867392
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27867392
    reference: chr 7
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1531A>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.732A>C
  hgvsp: ENST00000457186.2:c.732A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1995A>C
  hgvsp: ENST00000265393.6:c.1995A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1995A>C
  hgvsp: ENST00000543117.1:c.1995A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1524A>C
  hgvsp: ENST00000433216.2:c.1524A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2121A>C
  hgvsp: ENST00000396319.2:c.2121A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2193A>C
  hgvsp: ENST00000409980.1:c.2193A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7228
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6993
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6481
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5881
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2967
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6412
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3005
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36999
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3178
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro707Pro
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff

7-27867392-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27867392
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27867392
    reference: chr 7
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1524A>G
  hgvsp: ENST00000433216.2:c.1524A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1995A>G
  hgvsp: ENST00000543117.1:c.1995A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.732A>G
  hgvsp: ENST00000457186.2:c.732A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2193A>G
  hgvsp: ENST00000409980.1:c.2193A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1995A>G
  hgvsp: ENST00000265393.6:c.1995A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1531A>G
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2121A>G
  hgvsp: ENST00000396319.2:c.2121A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5881
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6412
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6481
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7228
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6993
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2967
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3178
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8828
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1642
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1492
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2726
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro707Pro
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum

7-27867394-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27867394
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27867394
    reference: chr 7
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2195G>A
  hgvsp: ENSP00000386515.1:p.Ser732Asn
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1533G>A
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1997G>A
  hgvsp: ENSP00000444811.1:p.Ser666Asn
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1526G>A
  hgvsp: ENSP00000391907.2:p.Ser509Asn
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2123G>A
  hgvsp: ENSP00000379612.2:p.Ser708Asn
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.734G>A
  hgvsp: ENSP00000412575.2:p.Ser245Asn
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1997G>A
  hgvsp: ENSP00000265393.6:p.Ser666Asn
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5881
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5745
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6481
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6992
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4531
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2969
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7227
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3005
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8825
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3178
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1492
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1643
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser708Asn
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum

7-27867394-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27867394
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27867394
    reference: chr 7
allele count: 4
allele frequency: 3.296304842271814e-5
allele num: 121348
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.1997G>C
  hgvsp: ENSP00000265393.6:p.Ser666Thr
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1526G>C
  hgvsp: ENSP00000391907.2:p.Ser509Thr
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.734G>C
  hgvsp: ENSP00000412575.2:p.Ser245Thr
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1533G>C
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2123G>C
  hgvsp: ENSP00000379612.2:p.Ser708Thr
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2195G>C
  hgvsp: ENSP00000386515.1:p.Ser732Thr
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.1997G>C
  hgvsp: ENSP00000444811.1:p.Ser666Thr
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4531
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2969
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6992
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6481
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5745
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6410
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5881
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7227
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2788
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8825
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3005
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1492
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3178
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser708Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

7-27867398-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27867398
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27867398
    reference: chr 7
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.738A>G
  hgvsp: ENST00000457186.2:c.738A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2199A>G
  hgvsp: ENST00000409980.1:c.2199A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2127A>G
  hgvsp: ENST00000396319.2:c.2127A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.2001A>G
  hgvsp: ENST00000265393.6:c.2001A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.2001A>G
  hgvsp: ENST00000543117.1:c.2001A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1530A>G
  hgvsp: ENST00000433216.2:c.1530A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1537A>G
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6992
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5746
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4531
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8823
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1643
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1492
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gln709Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD

7-27867400-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27867400
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 27867400
    reference: chr 7
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391907
  ensembl transcript: ENST00000433216
  gene symbol: TAX1BP1
  hgvsc: ENST00000433216.2:c.1532A>G
  hgvsp: ENSP00000391907.2:p.His511Arg
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000386515
  ensembl transcript: ENST00000409980
  gene symbol: TAX1BP1
  hgvsc: ENST00000409980.1:c.2201A>G
  hgvsp: ENSP00000386515.1:p.His734Arg
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000265393
  ensembl transcript: ENST00000265393
  gene symbol: TAX1BP1
  hgvsc: ENST00000265393.6:c.2003A>G
  hgvsp: ENSP00000265393.6:p.His668Arg
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000412575
  ensembl transcript: ENST00000457186
  gene symbol: TAX1BP1
  hgvsc: ENST00000457186.2:c.740A>G
  hgvsp: ENSP00000412575.2:p.His247Arg
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000379612
  ensembl transcript: ENST00000396319
  gene symbol: TAX1BP1
  hgvsc: ENST00000396319.2:c.2129A>G
  hgvsp: ENSP00000379612.2:p.His710Arg
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000444811
  ensembl transcript: ENST00000543117
  gene symbol: TAX1BP1
  hgvsc: ENST00000543117.1:c.2003A>G
  hgvsp: ENSP00000444811.1:p.His668Arg
  variant of: http://identifiers.org/hgnc/11575
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106052
  ensembl protein: ENSP00000391215
  ensembl transcript: ENST00000416801
  gene symbol: TAX1BP1
  hgvsc: ENST00000416801.2:c.*1539A>G
  variant of: http://identifiers.org/hgnc/11575
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5749
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6401
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6991
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.75e1
  variant carriers: 0
hgvs: p.His710Arg
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 3057
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 139
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4946
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21557
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7034
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2225
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14272
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.067224851352991e-5
allele num: 16482
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66636
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.47e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.57e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.93433e6

VQSLOD
type: SiteQuality
SIO_000300: 8.5e-1

QD
type: SiteQuality
SIO_000300: 9.81e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.733e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21520
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3231
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7029
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4121
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4940
bin: 7.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501411326647048e-5
allele num: 66604
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.59e-1

FS
type: SiteQuality
SIO_000300: 6.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.37e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.04e-1

DP
type: SiteQuality
SIO_000300: 1.933009e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.334e0

QD
type: SiteQuality
SIO_000300: 1.073e1

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3225
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2218
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4109
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3045
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4933
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503307276007216e-5
allele num: 66520
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.48e0

QD
type: SiteQuality
SIO_000300: 1.18e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.900000000000001e-3

DP
type: SiteQuality
SIO_000300: 1.93088e6

VQSLOD
type: SiteQuality
SIO_000300: 1.3e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.48e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.67e-1

GenotypeQuality
all individuals: 21430
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14275
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 7005
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2218
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3225
bin: 9.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66520
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.783021050196623e-4
allele num: 8646
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.48e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.900000000000001e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 6.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.07e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

QD
type: SiteQuality
SIO_000300: 1.18e1

DP
type: SiteQuality
SIO_000300: 1.93088e6

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14275
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 4097
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2214
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3223
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 2.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 11
allele frequency: 1.27344292660338e-3
allele num: 8638
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16174
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66330
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.45e0

MQRankSum
type: SiteQuality
SIO_000300: -1.9e-1

DP
type: SiteQuality
SIO_000300: 1.921371e6

VQSLOD
type: SiteQuality
SIO_000300: 1.93e0

QD
type: SiteQuality
SIO_000300: 1.382e1

MQ
type: SiteQuality
SIO_000300: 5.966e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

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

GenotypeQuality
all individuals: 4877
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6825
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2989
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2207
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66176
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.689607229753215e-5
allele num: 11508
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.316e1

MQRankSum
type: SiteQuality
SIO_000300: 4.92e-1

DP
type: SiteQuality
SIO_000300: 1.909688e6

MQ
type: SiteQuality
SIO_000300: 5.986e1

FS
type: SiteQuality
SIO_000300: 5.622e0

VQSLOD
type: SiteQuality
SIO_000300: 5.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.636e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.59e-1

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2204
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19959
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1652
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2956
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4855
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.918894716643214e-4
allele num: 15634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66034
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.257e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.229e0

MQRankSum
type: SiteQuality
SIO_000300: 1.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.33e-1

DP
type: SiteQuality
SIO_000300: 1.899092e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
all individuals: 95
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2203
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19716
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4074
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3221
bin: 9.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10252
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.639294827186268e-4
allele num: 8622
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.097801364670205e-5
allele num: 65950
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.059e0

QD
type: SiteQuality
SIO_000300: 1.466e1

MQ
type: SiteQuality
SIO_000300: 6.018e1

MQRankSum
type: SiteQuality
SIO_000300: 1.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.276e0

DP
type: SiteQuality
SIO_000300: 1.892593e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.879e0

GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65592
num of homozygotes: 0

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

South Asian
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allele count: 2
allele frequency: 1.359434475258292e-4
allele num: 14712
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10202
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 1.859481e6

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -6.67e-1

FS
type: SiteQuality
SIO_000300: 1.1418e1

QD
type: SiteQuality
SIO_000300: 1.049e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.94e-1

MQ
type: SiteQuality
SIO_000300: 5.949e1

VQSLOD
type: SiteQuality
SIO_000300: -2.001e0

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

South Asian
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allele count: 1
allele frequency: 6.888001102080176e-5
allele num: 14518
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65484
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10186
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 3.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.618e1

DP
type: SiteQuality
SIO_000300: 1.852708e6

BaseQRankSum
type: SiteQuality
SIO_000300: 7.26e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.31e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

FS
type: SiteQuality
SIO_000300: 4.841e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.6e-2

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

Latino
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allele frequency: 8.773469029654326e-5
allele num: 11398
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9972
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.647128074849743e-5
allele num: 64556
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 12474
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.001e0

QD
type: SiteQuality
SIO_000300: 1.643e1

MQRankSum
type: SiteQuality
SIO_000300: 2.56e0

MQ
type: SiteQuality
SIO_000300: 6.112e1

FS
type: SiteQuality
SIO_000300: 1.3774e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.14e-1

DP
type: SiteQuality
SIO_000300: 1.80964e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.817e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.5e-1

GenotypeQuality
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variant carriers: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9972
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64490
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.114248620577734e-5
allele num: 12324
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11402
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.32e0

DP
type: SiteQuality
SIO_000300: 1.80891e6

QD
type: SiteQuality
SIO_000300: 1.126e1

MQ
type: SiteQuality
SIO_000300: 6.026e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

GenotypeQuality
all individuals: 294
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variant carriers: 0

GenotypeQuality
all individuals: 3215
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11988
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.11332503113325e-5
allele num: 64240
num of homozygotes: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11398
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9888
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 3.058e1

DP
type: SiteQuality
SIO_000300: 1.80744e6

MQRankSum
type: SiteQuality
SIO_000300: 5.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.331e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

GenotypeQuality
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bin: 6.75e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11396
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12068
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64296
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6598
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DP
type: SiteQuality
SIO_000300: 1.80711e6

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 3.939e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.73e-1

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.067e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.47e-1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 11756
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9850
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64092
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11378
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

VQSLOD
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ReadPosRankSum
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FS
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MQ
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MQRankSum
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QD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8494
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.517680983457277e-5
allele num: 65890
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 9920
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16448
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.2e-2

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.215953307392996e-4
allele num: 16448
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65902
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8496
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Other
type: Population
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allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.73e-1

InbreedingCoeff
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VQSLOD
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QD
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 9.05e-1

DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4464
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4847
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1073
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3117
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16549
bin: 9.75e1
variant carriers: 9

South Asian
type: Population
allele count: 8
allele frequency: 4.863813229571985e-4
allele num: 16448
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8496
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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: 1.517404631118934e-5
allele num: 65902
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.39e0

QD
type: SiteQuality
SIO_000300: 1.356e1

FS
type: SiteQuality
SIO_000300: 9.05e-1

DP
type: SiteQuality
SIO_000300: 1.997319e6

MQRankSum
type: SiteQuality
SIO_000300: 4.14e-1

MQ
type: SiteQuality
SIO_000300: 5.944e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e0

GenotypeQuality
all individuals: 15358
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4572
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 281
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3614
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9932
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.0790273556231e-5
allele num: 16450
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.0e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.79e-1

FS
type: SiteQuality
SIO_000300: 6.073e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.43e-1

DP
type: SiteQuality
SIO_000300: 2.020044e6

QD
type: SiteQuality
SIO_000300: 1.131e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.11e0

GenotypeQuality
all individuals: 46
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3617
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3212
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6407
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16574
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 15385
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4591
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9940
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.076810889645114e-5
allele num: 16456
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65990
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

MQ
type: SiteQuality
SIO_000300: 5.952e1

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.302e0

VQSLOD
type: SiteQuality
SIO_000300: 7.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.83e-1

FS
type: SiteQuality
SIO_000300: 8.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.42e-1

QD
type: SiteQuality
SIO_000300: 1.363e1

DP
type: SiteQuality
SIO_000300: 2.021369e6

GenotypeQuality
all individuals: 131
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3231
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4628
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16579
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 812
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3634
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2444
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.17343346632246e-4
allele num: 8522
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66034
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9956
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.82e-1

MQ
type: SiteQuality
SIO_000300: 5.871e1

DP
type: SiteQuality
SIO_000300: 2.028627e6

FS
type: SiteQuality
SIO_000300: 1.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.921e0

QD
type: SiteQuality
SIO_000300: 1.093e1

VQSLOD
type: SiteQuality
SIO_000300: -5.438e-1

GenotypeQuality
all individuals: 265
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3663
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16369
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16603
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4696
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.001201441730076e-4
allele num: 9988
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66142
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.307e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

FS
type: SiteQuality
SIO_000300: 9.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

MQRankSum
type: SiteQuality
SIO_000300: 4.98e-1

DP
type: SiteQuality
SIO_000300: 2.036625e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.0e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.54e-1

GenotypeQuality
all individuals: 3665
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16607
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 6549
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16473
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2469
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5088
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4699
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.022609116189094e-5
allele num: 66168
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.613e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

QD
type: SiteQuality
SIO_000300: 1.255e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.65e0

VQSLOD
type: SiteQuality
SIO_000300: 8.03e-1

DP
type: SiteQuality
SIO_000300: 2.038629e6

MQRankSum
type: SiteQuality
SIO_000300: -2.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 5127
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16609
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 51
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16859
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3305
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3674
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.069434328720563e-5
allele num: 16476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66328
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10074
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.4e-2

FS
type: SiteQuality
SIO_000300: 7.529e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

VQSLOD
type: SiteQuality
SIO_000300: -8.740000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.428e0

MQ
type: SiteQuality
SIO_000300: 5.934e1

MQRankSum
type: SiteQuality
SIO_000300: -2.4e-2

QD
type: SiteQuality
SIO_000300: 1.115e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

DP
type: SiteQuality
SIO_000300: 2.04621e6

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

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 541
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3674
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2477
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3311
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16895
bin: 6.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10074
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507522537461935e-5
allele num: 66334
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.45e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.046633e6

MQRankSum
type: SiteQuality
SIO_000300: -8.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.55e-1

QD
type: SiteQuality
SIO_000300: 1.006e1

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16609
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6619
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4720
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2477
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.068697657482704e-5
allele num: 16478
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66334
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10074
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.006e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -8.9e-2

DP
type: SiteQuality
SIO_000300: 2.046633e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.63e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.7e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

GenotypeQuality
all individuals: 16963
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4720
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3673
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2477
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6630
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5132
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16609
bin: 9.75e1
variant carriers: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10090
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66364
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.069434328720563e-5
allele num: 16476
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 9.144e0

QD
type: SiteQuality
SIO_000300: 1.266e1

VQSLOD
type: SiteQuality
SIO_000300: -3.009e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.658e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.76e0

MQRankSum
type: SiteQuality
SIO_000300: 1.37e0

DP
type: SiteQuality
SIO_000300: 2.047156e6

MQ
type: SiteQuality
SIO_000300: 5.831e1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
all individuals: 2477
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6642
bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10126
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505933377507379e-5
allele num: 66404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e0

QD
type: SiteQuality
SIO_000300: 1.153e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.476e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.074e0

VQSLOD
type: SiteQuality
SIO_000300: 5.51e-1

FS
type: SiteQuality
SIO_000300: 7.47e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.16e-1

DP
type: SiteQuality
SIO_000300: 2.048687e6

MQ
type: SiteQuality
SIO_000300: 5.934e1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505615947484116e-5
allele num: 66418
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10142
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 7.6e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.049424e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.896e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 9.359999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e-1

GenotypeQuality
all individuals: 16615
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505434618974498e-5
allele num: 66426
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10142
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 2.631e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.120000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.049633e6

VQSLOD
type: SiteQuality
SIO_000300: -1.314e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.818e0

GenotypeQuality
all individuals: 114
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66484
num of homozygotes: 0

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

African
type: Population
allele count: 5
allele frequency: 4.910626595953643e-4
allele num: 10182
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 8.45e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.83e-1

QD
type: SiteQuality
SIO_000300: 1.442e1

DP
type: SiteQuality
SIO_000300: 2.051767e6

FS
type: SiteQuality
SIO_000300: 4.935e0

VQSLOD
type: SiteQuality
SIO_000300: 1.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.100000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.02e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503714174009804e-5
allele num: 66502
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10196
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -9.122e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.135e0

FS
type: SiteQuality
SIO_000300: 7.583e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.46e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.49e-1

QD
type: SiteQuality
SIO_000300: 1.724e1

DP
type: SiteQuality
SIO_000300: 2.052079e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.84e-1

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.508972855983407e-5
allele num: 66534
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 7.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.74e-1

FS
type: SiteQuality
SIO_000300: 7.216e0

DP
type: SiteQuality
SIO_000300: 2.054182e6

MQ
type: SiteQuality
SIO_000300: 5.977e1

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.27e1

VQSLOD
type: SiteQuality
SIO_000300: 6.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.48e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.503152206544582e-5
allele num: 66620
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.058479e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.33e-1

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.971e1

BaseQRankSum
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QD
type: SiteQuality
SIO_000300: 1.207e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.86e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

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

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
allele num: 8640
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South Asian
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allele count: 0
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allele num: 16506
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.059263e6

FS
type: SiteQuality
SIO_000300: 1.009e0

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.94e1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 9.18e-1

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 2.059649e6

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.824e0

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.959e1

QD
type: SiteQuality
SIO_000300: 1.516e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.1e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

Latino
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allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
allele num: 10356
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European (Non-Finnish)
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allele frequency: 1.500375093773443e-5
allele num: 66650
num of homozygotes: 0

Other
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num of homozygotes: 0

FS
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DP
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InbreedingCoeff
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MQRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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QD
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.285e0

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

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

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

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

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

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

South Asian
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allele frequency: 0.0e0
allele num: 16508
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European (Non-Finnish)
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allele frequency: 3.000840235265874e-5
allele num: 66648
num of homozygotes: 0

MQRankSum
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BaseQRankSum
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FS
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ClippingRankSum
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DP
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ReadPosRankSum
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
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VQSLOD
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SIO_000300: 5.679999999999999e-1

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

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

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

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

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

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

MQRankSum
type: SiteQuality
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FS
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QD
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ReadPosRankSum
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DP
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MQ
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BaseQRankSum
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.500105007350515e-5
allele num: 66662
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.500060002400096e-5
allele num: 66664
num of homozygotes: 0

Other
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num of homozygotes: 0

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

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

South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 9.63948332369385e-5
allele num: 10374
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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allele num: 6610
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InbreedingCoeff
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FS
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MQ
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QD
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MQRankSum
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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num of homozygotes: 0

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

Latino
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Other
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African
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South Asian
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European (Non-Finnish)
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allele frequency: 1.499970000599988e-5
allele num: 66668
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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Latino
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South Asian
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African
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 1.499970000599988e-5
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num of homozygotes: 0

DP
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FS
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BaseQRankSum
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MQ
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QD
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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Latino
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South Asian
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Other
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European (Non-Finnish)
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FS
type: SiteQuality
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VQSLOD
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QD
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DP
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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MQ
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BaseQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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European (Non-Finnish)
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European (Finnish)
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African
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Latino
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allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.909e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.71e-1

FS
type: SiteQuality
SIO_000300: 1.3373e1

MQRankSum
type: SiteQuality
SIO_000300: -3.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

BaseQRankSum
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SIO_000300: -3.201e0

VQSLOD
type: SiteQuality
SIO_000300: -1.841e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.12e-2

DP
type: SiteQuality
SIO_000300: 2.061069e6

QD
type: SiteQuality
SIO_000300: 1.143e1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.005530175522962e-5
allele num: 66544
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.42e0

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.17e-1

FS
type: SiteQuality
SIO_000300: 1.2017e1

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.78e0

VQSLOD
type: SiteQuality
SIO_000300: -2.416e0

DP
type: SiteQuality
SIO_000300: 2.053558e6

MQ
type: SiteQuality
SIO_000300: 5.975e1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16390
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503036132988637e-5
allele num: 66532
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -9.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.04e0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-2

QD
type: SiteQuality
SIO_000300: 1.322e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

DP
type: SiteQuality
SIO_000300: 2.052418e6

MQ
type: SiteQuality
SIO_000300: 5.911e1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 1
allele frequency: 8.683570684265369e-5
allele num: 11516
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66508
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16364
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.741e0

QD
type: SiteQuality
SIO_000300: 1.279e1

MQRankSum
type: SiteQuality
SIO_000300: 5.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.483e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.68e0

VQSLOD
type: SiteQuality
SIO_000300: 5.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 2.050434e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

MQ
type: SiteQuality
SIO_000300: 5.912e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 488
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GenotypeQuality
all individuals: 75
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507068149621726e-5
allele num: 66354
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16110
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: 1.63e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.134e0

DP
type: SiteQuality
SIO_000300: 2.022373e6

VQSLOD
type: SiteQuality
SIO_000300: -1.283e0

QD
type: SiteQuality
SIO_000300: 9.42e0

MQ
type: SiteQuality
SIO_000300: 5.878e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.913e0

MQRankSum
type: SiteQuality
SIO_000300: -5.91e-1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10314
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.268806419257773e-5
allele num: 15952
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66240
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.963e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.69e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -7.736e-1

MQRankSum
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DP
type: SiteQuality
SIO_000300: 1.999896e6

FS
type: SiteQuality
SIO_000300: 1.758e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.572e0

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.320313487548983e-5
allele num: 15822
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66176
num of homozygotes: 0

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

MQ
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ReadPosRankSum
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.228e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

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

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

South Asian
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allele count: 2
allele frequency: 1.271617497456765e-4
allele num: 15728
num of homozygotes: 0

East Asian
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allele count: 5
allele frequency: 5.804504295333178e-4
allele num: 8614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66146
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.941e1

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10252
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.493506493506494e-5
allele num: 15400
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66348
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16274
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 2
allele frequency: 1.740038280842179e-4
allele num: 11494
num of homozygotes: 0

African
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allele frequency: 9.695559433779329e-5
allele num: 10314
num of homozygotes: 0

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
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BaseQRankSum
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ReadPosRankSum
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MQ
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.195e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 470
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GenotypeQuality
all individuals: 3001
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2778
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2670
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6484
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507022725902707e-5
allele num: 66356
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16294
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 5.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

FS
type: SiteQuality
SIO_000300: 2.169e0

VQSLOD
type: SiteQuality
SIO_000300: 2.16e0

DP
type: SiteQuality
SIO_000300: 2.853308e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.45e-1

QD
type: SiteQuality
SIO_000300: 1.36e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.664e0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1645
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37012
bin: 9.75e1
variant carriers: 100

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

GenotypeQuality
all individuals: 2774
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2992
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2975
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 7
allele frequency: 6.08695652173913e-4
allele num: 11500
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.108647450110865e-3
allele num: 902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66354
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

African
type: Population
allele count: 92
allele frequency: 8.918185343156262e-3
allele num: 10316
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16318
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.974e1

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.85e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.92e0

DP
type: SiteQuality
SIO_000300: 2.861884e6

QD
type: SiteQuality
SIO_000300: 1.624e1

GenotypeQuality
all individuals: 88
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 291
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1473
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3048
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1646
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37008
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2784
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66418
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.223840411210378e-4
allele num: 16342
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.357e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.66e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.94e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.73e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e0

DP
type: SiteQuality
SIO_000300: 2.865695e6

GenotypeQuality
all individuals: 3121
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2998
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1652
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8398
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2787
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2727
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.665571235260003e-5
allele num: 10346
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66524
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.498e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

MQRankSum
type: SiteQuality
SIO_000300: 1.87e0

QD
type: SiteQuality
SIO_000300: 1.454e1

VQSLOD
type: SiteQuality
SIO_000300: 4.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 7.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.21e0

DP
type: SiteQuality
SIO_000300: 2.875181e6

GenotypeQuality
all individuals: 8398
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2727
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3121
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37006
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2998
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.680555555555556e-5
allele num: 11520
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66524
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: 6594
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.875181e6

MQRankSum
type: SiteQuality
SIO_000300: 1.87e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

FS
type: SiteQuality
SIO_000300: 1.498e0

QD
type: SiteQuality
SIO_000300: 1.454e1

MQ
type: SiteQuality
SIO_000300: 5.98e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.21e0

VQSLOD
type: SiteQuality
SIO_000300: 4.44e-1

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

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8680
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3148
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3001
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1484
bin: 7.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66616
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.665511265164645e-5
allele num: 11540
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.252e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -6.994e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.959e0

DP
type: SiteQuality
SIO_000300: 2.879365e6

FS
type: SiteQuality
SIO_000300: 2.571e0

MQRankSum
type: SiteQuality
SIO_000300: -9.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.68e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

QD
type: SiteQuality
SIO_000300: 1.032e1

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

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2789
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3001
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1646
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 37012
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8716
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3162
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.503902029055108e-5
allele num: 66632
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.333506673600277e-4
allele num: 11538
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-1

DP
type: SiteQuality
SIO_000300: 2.880496e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.09e-1

QD
type: SiteQuality
SIO_000300: 1.285e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 2.301e0

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.66e0

GenotypeQuality
all individuals: 3164
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2999
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1640
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8774
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37073
bin: 9.75e1
variant carriers: 107

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2780
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 95
allele frequency: 5.753391472868217e-3
allele num: 16512
num of homozygotes: 3

Other
type: Population
allele count: 4
allele frequency: 4.405286343612335e-3
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.923076923076923e-4
allele num: 10400
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.997720866070893e-5
allele num: 66692
num of homozygotes: 0

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

Latino
type: Population
allele count: 5
allele frequency: 4.332004851845434e-4
allele num: 11542
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.97e1

DP
type: SiteQuality
SIO_000300: 2.888104e6

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.09e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.25e-1

FS
type: SiteQuality
SIO_000300: 1.372e0

VQSLOD
type: SiteQuality
SIO_000300: 3.32e0

QD
type: SiteQuality
SIO_000300: 1.421e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

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

GenotypeQuality
all individuals: 8805
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1642
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2727
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2787
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37002
bin: 9.75e1
variant carriers: 1

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

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

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 4.93e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.72e-1

FS
type: SiteQuality
SIO_000300: 4.174e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.394e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.221e1

DP
type: SiteQuality
SIO_000300: 2.881688e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.07e-1

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1492
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1642
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37008
bin: 9.75e1
variant carriers: 21

GenotypeQuality
all individuals: 3004
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8813
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2787
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2727
bin: 7.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 8
allele frequency: 6.93000693000693e-4
allele num: 11544
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.49907057624273e-4
allele num: 66708
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.92e-1

FS
type: SiteQuality
SIO_000300: 5.620000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.06e-1

QD
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MQ
type: SiteQuality
SIO_000300: 5.964e1

InbreedingCoeff
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SIO_000300: 1.263e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.56e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.93e0

DP
type: SiteQuality
SIO_000300: 2.884009e6

GenotypeQuality
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variant carriers: 0

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

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

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

African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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South Asian
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allele count: 0
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allele num: 16512
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 908
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FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.749e-1

BaseQRankSum
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SIO_000300: -1.808e0

ReadPosRankSum
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QD
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.881888e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
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variant carriers: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11552
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.953e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.73e-1

QD
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MQRankSum
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SIO_000300: 1.92e0

ClippingRankSum
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SIO_000300: -1.012e0

DP
type: SiteQuality
SIO_000300: 2.882091e6

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 0

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

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

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

Other
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allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66716
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.92e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

QD
type: SiteQuality
SIO_000300: 1.005e1

VQSLOD
type: SiteQuality
SIO_000300: -7.554999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.012e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.882091e6

FS
type: SiteQuality
SIO_000300: 3.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.73e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

Other
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66714
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South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
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African
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.99e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.882401e6

InbreedingCoeff
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SIO_000300: 0.0e0

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.961e1

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.63e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.52e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
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East Asian
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allele count: 4
allele frequency: 4.624277456647399e-4
allele num: 8650
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
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Other
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South Asian
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.31e-1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

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

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

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

East Asian
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allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 5.96e-1

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