X-30864637-CTTAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030864637
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030864633
    reference: chr 0
allele count: 1
allele frequency: 1.348453997491876e-5
allele num: 74159
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1804+27_1804+30delATAA
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1804+27_1804+30delATAA
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1804+27_1804+30delATAA
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.*4_*7delATAA
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1804+27_1804+30delATAA
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.157+27_157+30delATAA
  variant of: http://identifiers.org/hgnc/30681
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 8.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 1.75e1
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genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 3.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 6.75e1
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genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 3.75e1
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genotype quality: GenotypeQuality
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  bin: 5.75e1
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genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
  all individuals: 1984
  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1262
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 11879
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: CTTAT
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP

X-30864643-GTTT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030864643
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030864640
    reference: chr 0
allele count: 1
allele frequency: 1.29881937318977e-5
allele num: 76993
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1804+22_1804+24delAAA
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1804+22_1804+24delAAA
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: coding_sequence_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1826_*1delAAA
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1804+22_1804+24delAAA
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.157+22_157+24delAAA
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1804+22_1804+24delAAA
  variant of: http://identifiers.org/hgnc/30681
canonical: false
consequence: coding sequence
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3428
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 425
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1450
  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 286
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: GTTT
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ

X-30864649-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030864649
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030864649
    reference: chr 0
allele count: 1
allele frequency: 1.258510678463107e-5
allele num: 79459
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1823G>A
  hgvsp: ENSP00000433193.1:p.Trp608Ter
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1804+19G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1804+19G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.157+19G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1804+19G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1804+19G>A
  variant of: http://identifiers.org/hgnc/30681
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 9.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Trp608Ter
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum

X-30864653-TAATC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030864653
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030864649
    reference: chr 0
allele count: 1
allele frequency: 1.236185625633545e-5
allele num: 80894
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1804+11_1804+14delGATT
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.157+11_157+14delGATT
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1804+11_1804+14delGATT
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1815_1818delGATT
  hgvsp: ENSP00000433193.1:p.Ile606PhefsTer5
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1804+11_1804+14delGATT
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1804+11_1804+14delGATT
  variant of: http://identifiers.org/hgnc/30681
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36830
  bin: 2.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 858
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1353
  bin: 7.25e1
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genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1755
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 4762
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ile606PhefsTer5
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: TAATC
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD

X-30864670-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030864670
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030864670
    reference: chr 0
allele count: 1
allele frequency: 1.178772661904425e-5
allele num: 84834
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1802G>C
  hgvsp: ENSP00000288422.2:p.Arg601Thr
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.155G>C
  hgvsp: ENSP00000368210.1:p.Arg52Thr
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1802G>C
  hgvsp: ENSP00000433193.1:p.Arg601Thr
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1802G>C
  hgvsp: ENSP00000368212.3:p.Arg601Thr
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1802G>C
  hgvsp: ENSP00000368214.2:p.Arg601Thr
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1802G>C
  hgvsp: ENSP00000368215.1:p.Arg601Thr
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8204
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40873
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2705
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2758
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2826
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41738
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1147
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg601Thr
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

X-30864676-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030864676
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030864676
    reference: chr 0
allele count: 1
allele frequency: 1.168497312456181e-5
allele num: 85580
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1796A>G
  hgvsp: ENSP00000368214.2:p.Gln599Arg
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.149A>G
  hgvsp: ENSP00000368210.1:p.Gln50Arg
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1796A>G
  hgvsp: ENSP00000433193.1:p.Gln599Arg
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1796A>G
  hgvsp: ENSP00000288422.2:p.Gln599Arg
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1796A>G
  hgvsp: ENSP00000368215.1:p.Gln599Arg
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1796A>G
  hgvsp: ENSP00000368212.3:p.Gln599Arg
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42786
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4306
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1795
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gln599Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

X-30864678-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030864678
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030864678
    reference: chr 0
allele count: 2
allele frequency: 2.331437097827101e-5
allele num: 85784
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.147T>C
  hgvsp: ENST00000378928.1:c.147T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1794T>C
  hgvsp: ENST00000378930.3:c.1794T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1794T>C
  hgvsp: ENST00000467136.1:c.1794T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1794T>C
  hgvsp: ENST00000378933.1:c.1794T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1794T>C
  hgvsp: ENST00000288422.2:c.1794T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1794T>C
  hgvsp: ENST00000378932.2:c.1794T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41749
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1151
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4765
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42984
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu598Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

X-30864678-AAGG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030864678
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030864675
    reference: chr 0
allele count: 1
allele frequency: 1.16571854891355e-5
allele num: 85784
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1791_1793delCCT
  hgvsp: ENSP00000368215.1:p.Leu598del
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1791_1793delCCT
  hgvsp: ENSP00000368212.3:p.Leu598del
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1791_1793delCCT
  hgvsp: ENSP00000288422.2:p.Leu598del
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.144_146delCCT
  hgvsp: ENSP00000368210.1:p.Leu49del
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1791_1793delCCT
  hgvsp: ENSP00000368214.2:p.Leu598del
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1791_1793delCCT
  hgvsp: ENSP00000433193.1:p.Leu598del
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41749
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4765
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4325
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42984
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1421
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1151
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu598del
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: AAGG
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ

X-30864688-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030864688
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030864688
    reference: chr 0
allele count: 2
allele frequency: 2.313770404562755e-5
allele num: 86439
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1784T>C
  hgvsp: ENSP00000288422.2:p.Val595Ala
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1784T>C
  hgvsp: ENSP00000368214.2:p.Val595Ala
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1784T>C
  hgvsp: ENSP00000368212.3:p.Val595Ala
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1784T>C
  hgvsp: ENSP00000368215.1:p.Val595Ala
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.137T>C
  hgvsp: ENSP00000368210.1:p.Val46Ala
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1784T>C
  hgvsp: ENSP00000433193.1:p.Val595Ala
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9015
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2762
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 42157
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1326
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1157
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4433
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1424
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val595Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum

X-30864699-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030864699
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030864699
    reference: chr 0
allele count: 1
allele frequency: 1.151383963524156e-5
allele num: 86852
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1773A>G
  hgvsp: ENST00000378933.1:c.1773A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1773A>G
  hgvsp: ENST00000378932.2:c.1773A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1773A>G
  hgvsp: ENST00000288422.2:c.1773A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1773A>G
  hgvsp: ENST00000378930.3:c.1773A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.126A>G
  hgvsp: ENST00000378928.1:c.126A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1773A>G
  hgvsp: ENST00000467136.1:c.1773A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42508
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4463
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 959
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1159
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4766
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1435
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr591Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

X-30864709-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030864709
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030864709
    reference: chr 0
allele count: 2
allele frequency: 2.300331247699669e-5
allele num: 86944
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.116T>C
  hgvsp: ENSP00000368210.1:p.Val39Ala
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1763T>C
  hgvsp: ENSP00000368215.1:p.Val588Ala
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1763T>C
  hgvsp: ENSP00000368214.2:p.Val588Ala
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1763T>C
  hgvsp: ENSP00000433193.1:p.Val588Ala
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1763T>C
  hgvsp: ENSP00000368212.3:p.Val588Ala
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1763T>C
  hgvsp: ENSP00000288422.2:p.Val588Ala
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4478
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 895
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1433
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44570
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
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genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1155
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val588Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum

X-30864745-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030864745
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030864745
    reference: chr 0
allele count: 1
allele frequency: 1.15944717558668e-5
allele num: 86248
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1727G>C
  hgvsp: ENSP00000368215.1:p.Arg576Thr
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1727G>C
  hgvsp: ENSP00000288422.2:p.Arg576Thr
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1727G>C
  hgvsp: ENSP00000433193.1:p.Arg576Thr
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.80G>C
  hgvsp: ENSP00000368210.1:p.Arg27Thr
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1727G>C
  hgvsp: ENSP00000368212.3:p.Arg576Thr
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1727G>C
  hgvsp: ENSP00000368214.2:p.Arg576Thr
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 422
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 107
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1420
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 206
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2257
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 647
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg576Thr
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP

X-30864752-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030864752
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030864752
    reference: chr 0
allele count: 1
allele frequency: 1.163968200388765e-5
allele num: 85913
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.73A>G
  hgvsp: ENSP00000368210.1:p.Met25Val
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1720A>G
  hgvsp: ENSP00000368215.1:p.Met574Val
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1720A>G
  hgvsp: ENSP00000288422.2:p.Met574Val
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1720A>G
  hgvsp: ENSP00000368212.3:p.Met574Val
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1720A>G
  hgvsp: ENSP00000368214.2:p.Met574Val
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1720A>G
  hgvsp: ENSP00000433193.1:p.Met574Val
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
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genotype depth: GenotypeDepth
  all individuals: 113
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 83
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genotype quality: GenotypeQuality
  all individuals: 386
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  variant carriers: 0
hgvs: p.Met574Val
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum

X-30864777-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030864777
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030864777
    reference: chr 0
allele count: 1
allele frequency: 1.189725530320155e-5
allele num: 84053
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1711-16G>C
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1711-16G>C
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.64-16G>C
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1711-16G>C
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1711-16G>C
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1711-16G>C
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 106
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1717
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 968
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

X-30864793-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030864793
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030864793
    reference: chr 0
allele count: 1
allele frequency: 1.20513871146569e-5
allele num: 82978
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1711-32C>T
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1711-32C>T
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1711-32C>T
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.64-32C>T
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1711-32C>T
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1711-32C>T
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7307
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 920
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD

X-30870846-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030870846
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030870846
    reference: chr 0
allele count: 1
allele frequency: 1.175944871704414e-5
allele num: 85038
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1710+49G>T
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1710+49G>T
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1710+49G>T
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1710+49G>T
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.63+49G>T
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1710+49G>T
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 2.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1235
  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 1966
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff

X-30870852-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030870852
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030870852
    reference: chr 0
allele count: 1
allele frequency: 1.172717890984145e-5
allele num: 85272
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1710+43T>C
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1710+43T>C
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.63+43T>C
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1710+43T>C
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1710+43T>C
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1710+43T>C
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1935
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genotype quality: GenotypeQuality
  all individuals: 31345
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2417
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genotype quality: GenotypeQuality
  all individuals: 1287
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  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD

X-30870858-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030870858
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030870858
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 85304
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.63+37G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1710+37G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1710+37G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1710+37G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1710+37G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1710+37G>A
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 19638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 208
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  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

X-30870859-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030870859
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030870859
    reference: chr 0
allele count: 1
allele frequency: 1.1707271386258e-5
allele num: 85417
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1710+36C>T
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1710+36C>T
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.63+36C>T
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1710+36C>T
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1710+36C>T
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1710+36C>T
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7457
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

X-30870862-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030870862
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030870862
    reference: chr 0
allele count: 1
allele frequency: 1.169221415459446e-5
allele num: 85527
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1710+33G>C
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.63+33G>C
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1710+33G>C
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1710+33G>C
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1710+33G>C
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1710+33G>C
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20305
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19942
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1078
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2211
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35018
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1308
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 4251
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2157
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 934
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

X-30870891-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030870891
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030870891
    reference: chr 0
allele count: 1
allele frequency: 1.154974475064101e-5
allele num: 86582
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1710+4A>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1710+4A>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.63+4A>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1710+4A>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1710+4A>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1710+4A>G
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21204
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7592
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22637
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1271
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38362
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
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genotype quality: GenotypeQuality
  all individuals: 445
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genotype quality: GenotypeQuality
  all individuals: 149
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2440
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
hgvs: c.1710+4A>G
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

X-30870901-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030870901
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030870901
    reference: chr 0
allele count: 3
allele frequency: 3.448870494912916e-5
allele num: 86985
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1704C>T
  hgvsp: ENST00000378932.2:c.1704C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1704C>T
  hgvsp: ENST00000288422.2:c.1704C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1704C>T
  hgvsp: ENST00000378933.1:c.1704C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.57C>T
  hgvsp: ENST00000378928.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1704C>T
  hgvsp: ENST00000467136.1:c.1704C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1704C>T
  hgvsp: ENST00000378930.3:c.1704C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 865
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2295
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 13
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7703
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genotype quality: GenotypeQuality
  all individuals: 1297
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile568Ile
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum

X-30870902-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030870902
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030870902
    reference: chr 0
allele count: 1
allele frequency: 1.149121496615837e-5
allele num: 87023
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1703T>C
  hgvsp: ENSP00000368212.3:p.Ile568Thr
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1703T>C
  hgvsp: ENSP00000288422.2:p.Ile568Thr
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1703T>C
  hgvsp: ENSP00000433193.1:p.Ile568Thr
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.56T>C
  hgvsp: ENSP00000368210.1:p.Ile19Thr
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1703T>C
  hgvsp: ENSP00000368215.1:p.Ile568Thr
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1703T>C
  hgvsp: ENSP00000368214.2:p.Ile568Thr
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21685
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23095
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39380
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7723
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 834
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ile568Thr
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

X-30870904-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030870904
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030870904
    reference: chr 0
allele count: 2
allele frequency: 2.297582942744233e-5
allele num: 87048
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1701G>T
  hgvsp: ENST00000288422.2:c.1701G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1701G>T
  hgvsp: ENST00000378933.1:c.1701G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1701G>T
  hgvsp: ENST00000467136.1:c.1701G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1701G>T
  hgvsp: ENST00000378930.3:c.1701G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1701G>T
  hgvsp: ENST00000378932.2:c.1701G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.54G>T
  hgvsp: ENST00000378928.1:c.54G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7667
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4253
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 781
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1297
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2295
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7714
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala567Ala
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

X-30870904-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030870904
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030870904
    reference: chr 0
allele count: 2
allele frequency: 2.297582942744233e-5
allele num: 87048
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1701G>A
  hgvsp: ENST00000378932.2:c.1701G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1701G>A
  hgvsp: ENST00000288422.2:c.1701G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.54G>A
  hgvsp: ENST00000378928.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1701G>A
  hgvsp: ENST00000378933.1:c.1701G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1701G>A
  hgvsp: ENST00000467136.1:c.1701G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1701G>A
  hgvsp: ENST00000378930.3:c.1701G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7667
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 781
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 693
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala567Ala
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

X-30870905-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030870905
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030870905
    reference: chr 0
allele count: 3
allele frequency: 3.443368073091227e-5
allele num: 87124
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1700C>T
  hgvsp: ENSP00000433193.1:p.Ala567Val
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1700C>T
  hgvsp: ENSP00000288422.2:p.Ala567Val
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.53C>T
  hgvsp: ENSP00000368210.1:p.Ala18Val
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1700C>T
  hgvsp: ENSP00000368212.3:p.Ala567Val
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1700C>T
  hgvsp: ENSP00000368215.1:p.Ala567Val
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1700C>T
  hgvsp: ENSP00000368214.2:p.Ala567Val
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21847
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23101
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1303
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2293
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4249
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala567Val
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff

X-30870948-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030870948
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030870948
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 87411
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1657G>A
  hgvsp: ENSP00000433193.1:p.Asp553Asn
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1657G>A
  hgvsp: ENSP00000368214.2:p.Asp553Asn
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1657G>A
  hgvsp: ENSP00000368215.1:p.Asp553Asn
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.10G>A
  hgvsp: ENSP00000368210.1:p.Asp4Asn
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1657G>A
  hgvsp: ENSP00000368212.3:p.Asp553Asn
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1657G>A
  hgvsp: ENSP00000288422.2:p.Asp553Asn
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22648
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2403
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2273
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7727
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp553Asn
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

X-30870971-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030870971
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030870971
    reference: chr 0
allele count: 64
allele frequency: 7.3439974296009e-4
allele num: 87146
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1634C>G
  hgvsp: ENSP00000288422.2:p.Ser545Cys
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1634C>G
  hgvsp: ENSP00000433193.1:p.Ser545Cys
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1634C>G
  hgvsp: ENSP00000368215.1:p.Ser545Cys
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.-14C>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1634C>G
  hgvsp: ENSP00000368212.3:p.Ser545Cys
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1634C>G
  hgvsp: ENSP00000368214.2:p.Ser545Cys
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7708
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 22428
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21611
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7469
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2360
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 38259
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser545Cys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum

X-30870976-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030870976
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030870976
    reference: chr 0
allele count: 1
allele frequency: 1.148408879497456e-5
allele num: 87077
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1629G>T
  hgvsp: ENSP00000288422.2:p.Leu543Phe
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1629G>T
  hgvsp: ENSP00000368214.2:p.Leu543Phe
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1629G>T
  hgvsp: ENSP00000368212.3:p.Leu543Phe
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1629G>T
  hgvsp: ENSP00000433193.1:p.Leu543Phe
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1629G>T
  hgvsp: ENSP00000368215.1:p.Leu543Phe
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.-19G>T
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21517
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38339
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4232
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1125
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu543Phe
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

X-30870980-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030870980
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030870980
    reference: chr 0
allele count: 3
allele frequency: 3.448355134600795e-5
allele num: 86998
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1625G>A
  hgvsp: ENSP00000368215.1:p.Arg542Gln
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.-23G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1625G>A
  hgvsp: ENSP00000368214.2:p.Arg542Gln
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1625G>A
  hgvsp: ENSP00000433193.1:p.Arg542Gln
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1625G>A
  hgvsp: ENSP00000368212.3:p.Arg542Gln
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1625G>A
  hgvsp: ENSP00000288422.2:p.Arg542Gln
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.75e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg542Gln
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

X-30870981-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030870981
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030870981
    reference: chr 0
allele count: 2
allele frequency: 2.299088411444862e-5
allele num: 86991
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368210
  ensembl transcript: ENST00000378928
  gene symbol: TAB3
  hgvsc: ENST00000378928.1:c.-24C>T
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1624C>T
  hgvsp: ENSP00000368212.3:p.Arg542Trp
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1624C>T
  hgvsp: ENSP00000288422.2:p.Arg542Trp
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1624C>T
  hgvsp: ENSP00000433193.1:p.Arg542Trp
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1624C>T
  hgvsp: ENSP00000368215.1:p.Arg542Trp
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1624C>T
  hgvsp: ENSP00000368214.2:p.Arg542Trp
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7699
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1260
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2350
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 480
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38268
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg542Trp
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

X-30871008-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030871008
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030871008
    reference: chr 0
allele count: 1
allele frequency: 1.157019056103854e-5
allele num: 86429
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1597C>T
  hgvsp: ENST00000288422.2:c.1597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1597C>T
  hgvsp: ENST00000378933.1:c.1597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1597C>T
  hgvsp: ENST00000378932.2:c.1597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1597C>T
  hgvsp: ENST00000378930.3:c.1597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1597C>T
  hgvsp: ENST00000467136.1:c.1597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 191
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7454
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 366
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 5.25e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 4228
  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 253
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genotype quality: GenotypeQuality
  all individuals: 461
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu533Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

X-30871008-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030871008
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030871008
    reference: chr 0
allele count: 1
allele frequency: 1.157019056103854e-5
allele num: 86429
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1597C>A
  hgvsp: ENSP00000368214.2:p.Leu533Met
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1597C>A
  hgvsp: ENSP00000288422.2:p.Leu533Met
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1597C>A
  hgvsp: ENSP00000368212.3:p.Leu533Met
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1597C>A
  hgvsp: ENSP00000433193.1:p.Leu533Met
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1597C>A
  hgvsp: ENSP00000368215.1:p.Leu533Met
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 6.75e1
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genotype depth: GenotypeDepth
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  bin: 4.25e1
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genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 12
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  variant carriers: 0
hgvs: p.Leu533Met
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

X-30871011-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030871011
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030871011
    reference: chr 0
allele count: 1
allele frequency: 1.158144652267068e-5
allele num: 86345
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1594C>A
  hgvsp: ENSP00000368214.2:p.Gln532Lys
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1594C>A
  hgvsp: ENSP00000368212.3:p.Gln532Lys
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1594C>A
  hgvsp: ENSP00000288422.2:p.Gln532Lys
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1594C>A
  hgvsp: ENSP00000368215.1:p.Gln532Lys
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1594C>A
  hgvsp: ENSP00000433193.1:p.Gln532Lys
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 6981
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  variant carriers: 0
hgvs: p.Gln532Lys
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: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

X-30871021-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030871021
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030871021
    reference: chr 0
allele count: 1
allele frequency: 1.164157906378421e-5
allele num: 85899
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1584G>A
  hgvsp: ENST00000378932.2:c.1584G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1584G>A
  hgvsp: ENST00000378933.1:c.1584G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1584G>A
  hgvsp: ENST00000378930.3:c.1584G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1584G>A
  hgvsp: ENST00000288422.2:c.1584G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1584G>A
  hgvsp: ENST00000467136.1:c.1584G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7359
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 720
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 484
  bin: 8.75e1
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genotype quality: GenotypeQuality
  all individuals: 2030
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1202
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 581
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36401
  bin: 6.25e1
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genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 6828
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg528Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum

X-30871038-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030871038
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030871038
    reference: chr 0
allele count: 1
allele frequency: 1.178425387996559e-5
allele num: 84859
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1567C>G
  hgvsp: ENSP00000368214.2:p.Arg523Gly
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1567C>G
  hgvsp: ENSP00000288422.2:p.Arg523Gly
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1567C>G
  hgvsp: ENSP00000433193.1:p.Arg523Gly
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1567C>G
  hgvsp: ENSP00000368212.3:p.Arg523Gly
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1567C>G
  hgvsp: ENSP00000368215.1:p.Arg523Gly
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7172
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3542
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19415
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20478
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 4.25e1
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genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 439
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genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
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genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 3.75e1
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genotype depth: GenotypeDepth
  all individuals: 130
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 834
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 48
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genotype quality: GenotypeQuality
  all individuals: 4209
  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 1170
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genotype quality: GenotypeQuality
  all individuals: 72
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg523Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

X-30871039-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030871039
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030871039
    reference: chr 0
allele count: 2
allele frequency: 2.358351512292907e-5
allele num: 84805
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1566A>G
  hgvsp: ENST00000467136.1:c.1566A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1566A>G
  hgvsp: ENST00000288422.2:c.1566A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1566A>G
  hgvsp: ENST00000378930.3:c.1566A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1566A>G
  hgvsp: ENST00000378933.1:c.1566A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1566A>G
  hgvsp: ENST00000378932.2:c.1566A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 75
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genotype depth: GenotypeDepth
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  bin: 4.75e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 276
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
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genotype depth: GenotypeDepth
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  bin: 2.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 869
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gln522Gln
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

X-30871059-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030871059
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030871059
    reference: chr 0
allele count: 23
allele frequency: 2.78831815922509e-4
allele num: 82487
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1550-4G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1550-4G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1550-4G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1550-4G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1550-4G>A
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9235
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 544
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  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2088
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: c.1550-4G>A
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

X-30871062-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030871062
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030871062
    reference: chr 0
allele count: 1
allele frequency: 1.217152107498874e-5
allele num: 82159
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1550-7G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1550-7G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1550-7G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1550-7G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1550-7G>A
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10234
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 5.25e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16810
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26781
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4189
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2360
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1683
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 960
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5557
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2341
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1122
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1947
  bin: 7.75e1
  variant carriers: 0
hgvs: c.1550-7G>A
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS

X-30871065-TATAG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030871065
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030871061
    reference: chr 0
allele count: 1
allele frequency: 1.220271144248252e-5
allele num: 81949
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1550-14_1550-11delCTAT
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1550-14_1550-11delCTAT
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1550-14_1550-11delCTAT
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1550-14_1550-11delCTAT
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1550-14_1550-11delCTAT
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5098
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16278
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11127
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6532
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5429
  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 525
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1672
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11400
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1087
  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 652
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2586
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1116
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: TATAG
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP

X-30871067-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030871067
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030871067
    reference: chr 0
allele count: 7
allele frequency: 8.564157776255261e-5
allele num: 81736
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1550-12A>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1550-12A>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1550-12A>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1550-12A>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1550-12A>G
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11819
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6499
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15935
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2811
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11906
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2705
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4190
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1107
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 650
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5375
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1159
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1922
  bin: 7.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

X-30871086-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030871086
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030871086
    reference: chr 0
allele count: 1
allele frequency: 1.267105930055753e-5
allele num: 78920
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1550-31C>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1550-31C>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1550-31C>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1550-31C>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1550-31C>G
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17720
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4745
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8732
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6750
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10253
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1396
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1199
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1148
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 972
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6450
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1229
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4176
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4469
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1197
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12151
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13843
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

X-30871094-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030871094
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030871094
    reference: chr 0
allele count: 3
allele frequency: 3.833033079075473e-5
allele num: 78267
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1550-39A>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1550-39A>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1550-39A>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1550-39A>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1550-39A>G
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8832
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7507
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10681
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.25e1
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num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum

X-30871095-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030871095
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030871095
    reference: chr 0
allele count: 1
allele frequency: 1.283120549175595e-5
allele num: 77935
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1550-40A>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1550-40A>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1550-40A>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1550-40A>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
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  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1550-40A>G
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
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X-30871101-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030871101
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030871101
    reference: chr 0
allele count: 1
allele frequency: 1.315408697482308e-5
allele num: 76022
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1550-46T>C
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1550-46T>C
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1550-46T>C
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1550-46T>C
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
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  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1550-46T>C
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS

X-30871103-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030871103
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030871103
    reference: chr 0
allele count: 2
allele frequency: 2.654773282361686e-5
allele num: 75336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1550-48G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1550-48G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1550-48G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1550-48G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1550-48G>A
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 330
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

X-30871104-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030871104
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030871104
    reference: chr 0
allele count: 1
allele frequency: 1.329769550936823e-5
allele num: 75201
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1550-49C>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1550-49C>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1550-49C>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1550-49C>G
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1550-49C>G
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

X-30872198-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872198
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872198
    reference: chr 0
allele count: 1
allele frequency: 1.593219258834401e-5
allele num: 62766
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1549+35G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1549+35G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1549+35G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1549+35G>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1549+35G>A
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 6021
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  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

X-30872199-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872199
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872199
    reference: chr 0
allele count: 1
allele frequency: 1.588688537612201e-5
allele num: 62945
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1549+34T>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1549+34T>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1549+34T>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1549+34T>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1549+34T>A
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3747
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD

X-30872213-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872213
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872213
    reference: chr 0
allele count: 1
allele frequency: 1.535320037461809e-5
allele num: 65133
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1549+20T>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1549+20T>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1549+20T>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1549+20T>A
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1549+20T>A
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

X-30872258-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872258
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872258
    reference: chr 0
allele count: 1
allele frequency: 1.242915382320772e-5
allele num: 80456
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1524A>T
  hgvsp: ENST00000378932.2:c.1524A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1524A>T
  hgvsp: ENST00000378933.1:c.1524A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1524A>T
  hgvsp: ENST00000288422.2:c.1524A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1524A>T
  hgvsp: ENST00000467136.1:c.1524A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1524A>T
  hgvsp: ENST00000378930.3:c.1524A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 383
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 4.25e1
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genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 275
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3372
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5340
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 866
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6741
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly508Gly
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

X-30872270-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872270
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872270
    reference: chr 0
allele count: 1
allele frequency: 1.212077136588973e-5
allele num: 82503
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1512T>C
  hgvsp: ENST00000378930.3:c.1512T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1512T>C
  hgvsp: ENST00000378932.2:c.1512T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1512T>C
  hgvsp: ENST00000467136.1:c.1512T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1512T>C
  hgvsp: ENST00000378933.1:c.1512T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1512T>C
  hgvsp: ENST00000288422.2:c.1512T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
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genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
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genotype depth: GenotypeDepth
  all individuals: 622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3933
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36530
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4862
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genotype depth: GenotypeDepth
  all individuals: 148
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 197
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genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
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genotype depth: GenotypeDepth
  all individuals: 310
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genotype depth: GenotypeDepth
  all individuals: 221
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3389
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genotype quality: GenotypeQuality
  all individuals: 460
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genotype quality: GenotypeQuality
  all individuals: 2179
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 464
  bin: 4.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 211
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genotype quality: GenotypeQuality
  all individuals: 122
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genotype quality: GenotypeQuality
  all individuals: 566
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser504Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-30872276-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872276
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872276
    reference: chr 0
allele count: 2
allele frequency: 2.40139280782854e-5
allele num: 83285
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1506G>A
  hgvsp: ENST00000288422.2:c.1506G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1506G>A
  hgvsp: ENST00000378930.3:c.1506G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1506G>A
  hgvsp: ENST00000467136.1:c.1506G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1506G>A
  hgvsp: ENST00000378932.2:c.1506G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1506G>A
  hgvsp: ENST00000378933.1:c.1506G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4089
  bin: 3.25e1
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genotype depth: GenotypeDepth
  all individuals: 630
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36920
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 884
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
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genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 390
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  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 310
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 87
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genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1857
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genotype quality: GenotypeQuality
  all individuals: 243
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genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gln502Gln
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-30872279-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872279
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872279
    reference: chr 0
allele count: 16
allele frequency: 1.910835632307453e-4
allele num: 83733
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1503T>C
  hgvsp: ENST00000467136.1:c.1503T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1503T>C
  hgvsp: ENST00000378933.1:c.1503T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1503T>C
  hgvsp: ENST00000288422.2:c.1503T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1503T>C
  hgvsp: ENST00000378932.2:c.1503T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1503T>C
  hgvsp: ENST00000378930.3:c.1503T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4168
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9663
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  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1195
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
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  variant carriers: 2
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
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  variant carriers: 2
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 2
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 221
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
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  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4029
  bin: 2.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 443
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Tyr501Tyr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

X-30872289-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872289
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872289
    reference: chr 0
allele count: 1
allele frequency: 1.177052190494127e-5
allele num: 84958
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1493G>C
  hgvsp: ENSP00000368212.3:p.Ser498Thr
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1493G>C
  hgvsp: ENSP00000433193.1:p.Ser498Thr
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1493G>C
  hgvsp: ENSP00000368214.2:p.Ser498Thr
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1493G>C
  hgvsp: ENSP00000288422.2:p.Ser498Thr
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1493G>C
  hgvsp: ENSP00000368215.1:p.Ser498Thr
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 940
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35820
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2362
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6097
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2809
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser498Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

X-30872292-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872292
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872292
    reference: chr 0
allele count: 1901
allele frequency: 2.28416942024632e-2
allele num: 83225
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1490G>A
  hgvsp: ENSP00000433193.1:p.Gly497Glu
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1490G>A
  hgvsp: ENSP00000368212.3:p.Gly497Glu
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1490G>A
  hgvsp: ENSP00000288422.2:p.Gly497Glu
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1490G>A
  hgvsp: ENSP00000368215.1:p.Gly497Glu
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1490G>A
  hgvsp: ENSP00000368214.2:p.Gly497Glu
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 4.75e1
  variant carriers: 286
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 3.25e1
  variant carriers: 203
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 3.75e1
  variant carriers: 247
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 9821
  bin: 2.75e1
  variant carriers: 175
genotype depth: GenotypeDepth
  all individuals: 35873
  bin: 2.25e1
  variant carriers: 107
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 6.75e1
  variant carriers: 148
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.25e1
  variant carriers: 175
genotype depth: GenotypeDepth
  all individuals: 2124
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 4.25e1
  variant carriers: 263
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 1.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 1.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.25e1
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 212
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.75e1
  variant carriers: 99
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 9.75e1
  variant carriers: 553
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.25e1
  variant carriers: 273
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.25e1
  variant carriers: 91
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 4.75e1
  variant carriers: 105
genotype quality: GenotypeQuality
  all individuals: 34296
  bin: 6.25e1
  variant carriers: 91
genotype quality: GenotypeQuality
  all individuals: 825
  bin: 8.75e1
  variant carriers: 95
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 3.25e1
  variant carriers: 77
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 7.5e0
  variant carriers: 51
genotype quality: GenotypeQuality
  all individuals: 1886
  bin: 8.25e1
  variant carriers: 87
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 3.75e1
  variant carriers: 92
genotype quality: GenotypeQuality
  all individuals: 2879
  bin: 7.75e1
  variant carriers: 90
genotype quality: GenotypeQuality
  all individuals: 2407
  bin: 2.25e1
  variant carriers: 64
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 4.25e1
  variant carriers: 95
genotype quality: GenotypeQuality
  all individuals: 1197
  bin: 2.5e0
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 5800
  bin: 6.75e1
  variant carriers: 110
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 5.75e1
  variant carriers: 91
hgvs: p.Gly497Glu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

X-30872299-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872299
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872299
    reference: chr 0
allele count: 22
allele frequency: 2.556445146821293e-4
allele num: 86057
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1483G>A
  hgvsp: ENSP00000288422.2:p.Glu495Lys
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1483G>A
  hgvsp: ENSP00000368215.1:p.Glu495Lys
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1483G>A
  hgvsp: ENSP00000368214.2:p.Glu495Lys
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1483G>A
  hgvsp: ENSP00000433193.1:p.Glu495Lys
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1483G>A
  hgvsp: ENSP00000368212.3:p.Glu495Lys
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 4719
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 279
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  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10316
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36288
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35661
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1685
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1016
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3111
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2098
  bin: 8.25e1
  variant carriers: 1
hgvs: p.Glu495Lys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

X-30872301-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872301
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872301
    reference: chr 0
allele count: 4
allele frequency: 4.631827603376602e-5
allele num: 86359
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1481G>C
  hgvsp: ENSP00000368214.2:p.Gly494Ala
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1481G>C
  hgvsp: ENSP00000368215.1:p.Gly494Ala
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1481G>C
  hgvsp: ENSP00000288422.2:p.Gly494Ala
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1481G>C
  hgvsp: ENSP00000433193.1:p.Gly494Ala
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1481G>C
  hgvsp: ENSP00000368212.3:p.Gly494Ala
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10483
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36291
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4774
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 939
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1518
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3189
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly494Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

X-30872305-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872305
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872305
    reference: chr 0
allele count: 1
allele frequency: 1.15350897429982e-5
allele num: 86692
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1477G>C
  hgvsp: ENSP00000433193.1:p.Gly493Arg
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1477G>C
  hgvsp: ENSP00000368212.3:p.Gly493Arg
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1477G>C
  hgvsp: ENSP00000288422.2:p.Gly493Arg
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1477G>C
  hgvsp: ENSP00000368215.1:p.Gly493Arg
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1477G>C
  hgvsp: ENSP00000368214.2:p.Gly493Arg
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 4.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 36397
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 187
  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 118
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly493Arg
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

X-30872305-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872305
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872305
    reference: chr 0
allele count: 1
allele frequency: 1.15350897429982e-5
allele num: 86692
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1477G>A
  hgvsp: ENSP00000368212.3:p.Gly493Arg
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1477G>A
  hgvsp: ENSP00000433193.1:p.Gly493Arg
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1477G>A
  hgvsp: ENSP00000368215.1:p.Gly493Arg
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1477G>A
  hgvsp: ENSP00000368214.2:p.Gly493Arg
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1477G>A
  hgvsp: ENSP00000288422.2:p.Gly493Arg
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4880
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly493Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

X-30872307-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872307
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872307
    reference: chr 0
allele count: 1
allele frequency: 1.151436993367723e-5
allele num: 86848
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1475C>A
  hgvsp: ENSP00000368214.2:p.Ser492Tyr
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1475C>A
  hgvsp: ENSP00000433193.1:p.Ser492Tyr
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1475C>A
  hgvsp: ENSP00000288422.2:p.Ser492Tyr
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1475C>A
  hgvsp: ENSP00000368215.1:p.Ser492Tyr
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1475C>A
  hgvsp: ENSP00000368212.3:p.Ser492Tyr
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 213
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Ser492Tyr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

X-30872317-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872317
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872317
    reference: chr 0
allele count: 1
allele frequency: 1.145265472536534e-5
allele num: 87316
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1465A>G
  hgvsp: ENSP00000368215.1:p.Ile489Val
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1465A>G
  hgvsp: ENSP00000433193.1:p.Ile489Val
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1465A>G
  hgvsp: ENSP00000368214.2:p.Ile489Val
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1465A>G
  hgvsp: ENSP00000368212.3:p.Ile489Val
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1465A>G
  hgvsp: ENSP00000288422.2:p.Ile489Val
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 143
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Ile489Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

X-30872331-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872331
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872331
    reference: chr 0
allele count: 1
allele frequency: 1.142139226771743e-5
allele num: 87555
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1451A>G
  hgvsp: ENSP00000368212.3:p.Gln484Arg
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1451A>G
  hgvsp: ENSP00000288422.2:p.Gln484Arg
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1451A>G
  hgvsp: ENSP00000368214.2:p.Gln484Arg
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1451A>G
  hgvsp: ENSP00000433193.1:p.Gln484Arg
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1451A>G
  hgvsp: ENSP00000368215.1:p.Gln484Arg
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11323
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36978
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5206
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37589
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1111
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1002
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3454
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gln484Arg
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

X-30872339-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872339
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872339
    reference: chr 0
allele count: 2
allele frequency: 2.282401542903443e-5
allele num: 87627
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1443A>T
  hgvsp: ENSP00000368212.3:p.Glu481Asp
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1443A>T
  hgvsp: ENSP00000433193.1:p.Glu481Asp
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1443A>T
  hgvsp: ENSP00000288422.2:p.Glu481Asp
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1443A>T
  hgvsp: ENSP00000368214.2:p.Glu481Asp
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1443A>T
  hgvsp: ENSP00000368215.1:p.Glu481Asp
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 143
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 5322
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genotype quality: GenotypeQuality
  all individuals: 3
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1004
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37659
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3462
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Glu481Asp
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP

X-30872355-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872355
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872355
    reference: chr 0
allele count: 3
allele frequency: 3.42168894566358e-5
allele num: 87676
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1427G>A
  hgvsp: ENSP00000368215.1:p.Arg476His
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1427G>A
  hgvsp: ENSP00000288422.2:p.Arg476His
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1427G>A
  hgvsp: ENSP00000368214.2:p.Arg476His
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1427G>A
  hgvsp: ENSP00000368212.3:p.Arg476His
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1427G>A
  hgvsp: ENSP00000433193.1:p.Arg476His
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 394
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11467
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg476His
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP

X-30872356-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872356
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872356
    reference: chr 0
allele count: 4
allele frequency: 4.562199892788303e-5
allele num: 87677
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1426C>T
  hgvsp: ENSP00000368212.3:p.Arg476Cys
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1426C>T
  hgvsp: ENSP00000368215.1:p.Arg476Cys
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1426C>T
  hgvsp: ENSP00000288422.2:p.Arg476Cys
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1426C>T
  hgvsp: ENSP00000433193.1:p.Arg476Cys
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1426C>T
  hgvsp: ENSP00000368214.2:p.Arg476Cys
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11480
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 1025
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genotype depth: GenotypeDepth
  all individuals: 329
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  variant carriers: 1
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3478
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genotype quality: GenotypeQuality
  all individuals: 2743
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg476Cys
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

X-30872356-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872356
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872356
    reference: chr 0
allele count: 1
allele frequency: 1.140549973197076e-5
allele num: 87677
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1426C>G
  hgvsp: ENSP00000433193.1:p.Arg476Gly
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1426C>G
  hgvsp: ENSP00000288422.2:p.Arg476Gly
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1426C>G
  hgvsp: ENSP00000368215.1:p.Arg476Gly
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1426C>G
  hgvsp: ENSP00000368212.3:p.Arg476Gly
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1426C>G
  hgvsp: ENSP00000368214.2:p.Arg476Gly
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3478
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37611
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1011
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg476Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

X-30872385-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872385
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872385
    reference: chr 0
allele count: 1
allele frequency: 1.140966398539563e-5
allele num: 87645
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1397A>G
  hgvsp: ENSP00000368212.3:p.Asn466Ser
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1397A>G
  hgvsp: ENSP00000368214.2:p.Asn466Ser
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1397A>G
  hgvsp: ENSP00000433193.1:p.Asn466Ser
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1397A>G
  hgvsp: ENSP00000368215.1:p.Asn466Ser
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1397A>G
  hgvsp: ENSP00000288422.2:p.Asn466Ser
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11491
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 577
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genotype depth: GenotypeDepth
  all individuals: 143
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genotype depth: GenotypeDepth
  all individuals: 365
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 105
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 78
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
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genotype quality: GenotypeQuality
  all individuals: 97
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3490
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1122
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asn466Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff

X-30872393-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872393
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872393
    reference: chr 0
allele count: 1
allele frequency: 1.141278917154563e-5
allele num: 87621
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1389G>A
  hgvsp: ENST00000378933.1:c.1389G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1389G>A
  hgvsp: ENST00000378932.2:c.1389G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1389G>A
  hgvsp: ENST00000378930.3:c.1389G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1389G>A
  hgvsp: ENST00000288422.2:c.1389G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1389G>A
  hgvsp: ENST00000467136.1:c.1389G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36068
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5350
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 485
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 5346
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1019
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr463Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

X-30872394-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872394
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872394
    reference: chr 0
allele count: 1
allele frequency: 1.141226818830243e-5
allele num: 87625
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1388C>T
  hgvsp: ENSP00000368215.1:p.Thr463Met
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1388C>T
  hgvsp: ENSP00000368214.2:p.Thr463Met
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1388C>T
  hgvsp: ENSP00000368212.3:p.Thr463Met
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1388C>T
  hgvsp: ENSP00000433193.1:p.Thr463Met
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1388C>T
  hgvsp: ENSP00000288422.2:p.Thr463Met
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36060
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11500
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 5346
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genotype quality: GenotypeQuality
  all individuals: 3497
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 6
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6718
  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 164
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genotype quality: GenotypeQuality
  all individuals: 148
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr463Met
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

X-30872400-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872400
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872400
    reference: chr 0
allele count: 3
allele frequency: 3.424813918443764e-5
allele num: 87596
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1382G>A
  hgvsp: ENSP00000368215.1:p.Arg461Gln
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1382G>A
  hgvsp: ENSP00000288422.2:p.Arg461Gln
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1382G>A
  hgvsp: ENSP00000368212.3:p.Arg461Gln
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1382G>A
  hgvsp: ENSP00000433193.1:p.Arg461Gln
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1382G>A
  hgvsp: ENSP00000368214.2:p.Arg461Gln
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35759
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5350
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11419
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1023
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5353
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 36219
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6707
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3497
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg461Gln
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

X-30872407-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872407
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872407
    reference: chr 0
allele count: 3
allele frequency: 3.425204941428996e-5
allele num: 87586
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1375G>A
  hgvsp: ENSP00000368215.1:p.Val459Ile
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1375G>A
  hgvsp: ENSP00000433193.1:p.Val459Ile
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1375G>A
  hgvsp: ENSP00000368214.2:p.Val459Ile
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1375G>A
  hgvsp: ENSP00000368212.3:p.Val459Ile
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1375G>A
  hgvsp: ENSP00000288422.2:p.Val459Ile
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11388
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2393
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6712
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35929
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2742
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1129
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5364
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val459Ile
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

X-30872408-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872408
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872408
    reference: chr 0
allele count: 1
allele frequency: 1.141734980476332e-5
allele num: 87586
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1374C>T
  hgvsp: ENST00000288422.2:c.1374C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1374C>T
  hgvsp: ENST00000378930.3:c.1374C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1374C>T
  hgvsp: ENST00000378933.1:c.1374C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1374C>T
  hgvsp: ENST00000467136.1:c.1374C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1374C>T
  hgvsp: ENST00000378932.2:c.1374C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5344
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35533
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35932
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2742
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5365
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3504
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr458Thr
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

X-30872422-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24030872422
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24030872422
    reference: chr 0
allele count: 1
allele frequency: 1.142400182784029e-5
allele num: 87535
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368214
  ensembl transcript: ENST00000378932
  gene symbol: TAB3
  hgvsc: ENST00000378932.2:c.1360G>T
  hgvsp: ENSP00000368214.2:p.Val454Phe
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368212
  ensembl transcript: ENST00000378930
  gene symbol: TAB3
  hgvsc: ENST00000378930.3:c.1360G>T
  hgvsp: ENSP00000368212.3:p.Val454Phe
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000368215
  ensembl transcript: ENST00000378933
  gene symbol: TAB3
  hgvsc: ENST00000378933.1:c.1360G>T
  hgvsp: ENSP00000368215.1:p.Val454Phe
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000288422
  ensembl transcript: ENST00000288422
  gene symbol: TAB3
  hgvsc: ENST00000288422.2:c.1360G>T
  hgvsp: ENSP00000288422.2:p.Val454Phe
  variant of: http://identifiers.org/hgnc/30681
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157625
  ensembl protein: ENSP00000433193
  ensembl transcript: ENST00000467136
  gene symbol: TAB3
  hgvsc: ENST00000467136.1:c.1360G>T
  hgvsp: ENSP00000433193.1:p.Val454Phe
  variant of: http://identifiers.org/hgnc/30681
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35218
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1132
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6692
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35479
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5369
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val454Phe
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 27603
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3576
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4759
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 510
bin: 7.5e0
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6030
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7984
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4169
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6131
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8523
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 517
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.450680063717681e-5
allele num: 40805
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.101e1

MQ
type: SiteQuality
SIO_000300: 5.896e1

VQSLOD
type: SiteQuality
SIO_000300: 3.34e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

DP
type: SiteQuality
SIO_000300: 1.412364e6

GenotypeQuality
all individuals: 1144
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1289
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31569
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 544
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6198
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6626
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8769
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4261
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8116
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.354104380988253e-5
allele num: 42479
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.466865e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

QD
type: SiteQuality
SIO_000300: 3.326e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.08e0

MQ
type: SiteQuality
SIO_000300: 3.686e1

GenotypeQuality
all individuals: 34515
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1739
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.213592233009709e-4
allele num: 8240
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7068
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6334
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43972
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8943
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4342
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.407e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.26e-1

DP
type: SiteQuality
SIO_000300: 1.514961e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.824e1

QD
type: SiteQuality
SIO_000300: 1.149e1

MQRankSum
type: SiteQuality
SIO_000300: -1.518e0

GenotypeQuality
all individuals: 542
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3958
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6396
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8298
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.232740912744485e-5
allele num: 44788
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9014
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6420
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7420
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4386
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.22e0

DP
type: SiteQuality
SIO_000300: 1.539211e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQ
type: SiteQuality
SIO_000300: 5.802e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.92e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.662e1

GenotypeQuality
all individuals: 188
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1783
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4230
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1390
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6583
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8431
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.133743011991636e-5
allele num: 46866
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4478
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9194
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 605
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8677
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.265e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.16e-2

DP
type: SiteQuality
SIO_000300: 1.615501e6

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

VQSLOD
type: SiteQuality
SIO_000300: -4.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.33e0

QD
type: SiteQuality
SIO_000300: 3.435e1

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4765
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 234
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2127
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1155
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1422
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47192
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9002
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8451
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.083893344894862e-4
allele num: 9226
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4491
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.393e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.39e-1

DP
type: SiteQuality
SIO_000300: 1.630278e6

MQRankSum
type: SiteQuality
SIO_000300: -9.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.909999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.5e0

QD
type: SiteQuality
SIO_000300: 1.524e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.922e1

GenotypeQuality
all individuals: 1797
bin: 7.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 131
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1933
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1421
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4325
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9094
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9235
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.230118443316413e-5
allele num: 47280
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8458
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4491
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.56e-2

DP
type: SiteQuality
SIO_000300: 1.634544e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.43e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

QD
type: SiteQuality
SIO_000300: 2.275e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.45e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1933
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1797
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 187
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9094
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8458
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.08283703302653e-4
allele num: 9235
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4491
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47280
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.56e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.43e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

DP
type: SiteQuality
SIO_000300: 1.634544e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.45e0

QD
type: SiteQuality
SIO_000300: 2.275e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 169
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 43879
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1813
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47559
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9261
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.180219520830875e-4
allele num: 8473
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4500
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9410
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.511030522816561e-4
allele num: 6618
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.819e-1

QD
type: SiteQuality
SIO_000300: 6.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

DP
type: SiteQuality
SIO_000300: 1.648957e6

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.600000000000001e-1

FS
type: SiteQuality
SIO_000300: 3.1e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.89e0

MQRankSum
type: SiteQuality
SIO_000300: 5.55e-1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8487
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4514
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9282
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.040366208905535e-4
allele num: 9612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47710
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6627
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.95e-1

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.1e-1

DP
type: SiteQuality
SIO_000300: 1.657368e6

QD
type: SiteQuality
SIO_000300: 7.97e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4766
bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9284
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9646
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.017501508750754e-4
allele num: 6628
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4515
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8487
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47762
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 1.276e1

VQSLOD
type: SiteQuality
SIO_000300: 2.28e0

MQRankSum
type: SiteQuality
SIO_000300: 8.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.75e-1

FS
type: SiteQuality
SIO_000300: 1.106e0

DP
type: SiteQuality
SIO_000300: 1.6605e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.41e0

GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4340
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4766
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 484
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1791
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42394
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8479
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9164
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9281
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6625
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.102297811507978e-5
allele num: 47567
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4516
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.007e0

QD
type: SiteQuality
SIO_000300: 1.392e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

VQSLOD
type: SiteQuality
SIO_000300: -4.518e-1

FS
type: SiteQuality
SIO_000300: 2.428e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.85e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.778e0

DP
type: SiteQuality
SIO_000300: 1.639813e6

GenotypeQuality
all individuals: 139
bin: 5.75e1
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
all individuals: 4766
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variant carriers: 1

GenotypeQuality
all individuals: 484
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variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 647
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GenotypeQuality
all individuals: 1143
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 615
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9275
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8970
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.107570392851121e-5
allele num: 47448
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6621
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4514
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.784e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.92e0

FS
type: SiteQuality
SIO_000300: 3.874e0

DP
type: SiteQuality
SIO_000300: 1.629652e6

MQRankSum
type: SiteQuality
SIO_000300: 7.25e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.081e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.199e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e0

GenotypeQuality
all individuals: 69
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1747
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 483
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variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4765
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variant carriers: 1

GenotypeQuality
all individuals: 34760
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variant carriers: 0

GenotypeQuality
all individuals: 1730
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variant carriers: 0

GenotypeQuality
all individuals: 1133
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.189343482397717e-4
allele num: 8408
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9210
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6573
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 599
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8062
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46708
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4493
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.839e0

QD
type: SiteQuality
SIO_000300: 1.175e1

MQRankSum
type: SiteQuality
SIO_000300: 4.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 1.555505e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e0

GenotypeQuality
all individuals: 976
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2453
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 411
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variant carriers: 0

GenotypeQuality
all individuals: 3643
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variant carriers: 0

GenotypeQuality
all individuals: 4763
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variant carriers: 1

GenotypeQuality
all individuals: 647
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6527
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7579
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.162068667300873e-5
allele num: 46252
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9174
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4478
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.11e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

DP
type: SiteQuality
SIO_000300: 1.478987e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.328e0

FS
type: SiteQuality
SIO_000300: 6.894e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.81e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

QD
type: SiteQuality
SIO_000300: 8.99e0

GenotypeQuality
all individuals: 104
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2154
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2610
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 808
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variant carriers: 0

GenotypeQuality
all individuals: 1354
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2620
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variant carriers: 0

GenotypeQuality
all individuals: 7053
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variant carriers: 0

GenotypeQuality
all individuals: 2254
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 603
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.119452333517019e-5
allele num: 47182
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4488
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9250
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8447
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.953e1

DP
type: SiteQuality
SIO_000300: 1.587384e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.19e-2

GenotypeQuality
all individuals: 942
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
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variant carriers: 0

GenotypeQuality
all individuals: 36
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GenotypeQuality
all individuals: 1469
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variant carriers: 0

GenotypeQuality
all individuals: 614
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variant carriers: 0

GenotypeQuality
all individuals: 507
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variant carriers: 0

GenotypeQuality
all individuals: 212
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variant carriers: 0

GenotypeQuality
all individuals: 4252
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4495
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9258
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.183431952662722e-4
allele num: 8450
num of homozygotes: 0

South 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: 47289
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.01e-1

DP
type: SiteQuality
SIO_000300: 1.605895e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e0

MQ
type: SiteQuality
SIO_000300: 5.887e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.89e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 1.571e1

GenotypeQuality
all individuals: 776
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2191
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1575
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 507
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variant carriers: 0

GenotypeQuality
all individuals: 122
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variant carriers: 0

GenotypeQuality
all individuals: 2227
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 696
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GenotypeQuality
all individuals: 1277
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 607
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4491
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9258
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8449
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6587
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47296
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.45e-2

DP
type: SiteQuality
SIO_000300: 1.624461e6

FS
type: SiteQuality
SIO_000300: 2.692e0

MQ
type: SiteQuality
SIO_000300: 5.919e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.799e0

MQRankSum
type: SiteQuality
SIO_000300: 6.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 566
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GenotypeQuality
all individuals: 208
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2392
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8677
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6597
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47328
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.08038029386344e-4
allele num: 9256
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8455
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4498
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

QD
type: SiteQuality
SIO_000300: 1.063e1

FS
type: SiteQuality
SIO_000300: 2.572e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.16e-1

DP
type: SiteQuality
SIO_000300: 1.628745e6

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 64
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variant carriers: 0

GenotypeQuality
all individuals: 2392
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1278
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.181893393215932e-4
allele num: 8461
num of homozygotes: 0

East Asian
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: 47379
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8719
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4498
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9261
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 609
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.55e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.626e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.61e0

MQ
type: SiteQuality
SIO_000300: 5.933e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.71e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.338e0

DP
type: SiteQuality
SIO_000300: 1.637619e6

GenotypeQuality
all individuals: 7645
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4251
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 695
bin: 9.25e1
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GenotypeQuality
all individuals: 133
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8489
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4513
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47672
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9287
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 619
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.509661835748792e-4
allele num: 6624
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9378
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.68e-2

MQ
type: SiteQuality
SIO_000300: 5.922e1

QD
type: SiteQuality
SIO_000300: 1.15e1

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.072e0

VQSLOD
type: SiteQuality
SIO_000300: 2.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

DP
type: SiteQuality
SIO_000300: 1.683699e6

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
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GenotypeQuality
all individuals: 16
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GenotypeQuality
all individuals: 695
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GenotypeQuality
all individuals: 4253
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 136
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GenotypeQuality
all individuals: 507
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2444
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8495
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 623
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9295
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4517
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 4.528301886792453e-4
allele num: 6625
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9673
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47757
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -9.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

VQSLOD
type: SiteQuality
SIO_000300: 2.45e0

DP
type: SiteQuality
SIO_000300: 1.696864e6

QD
type: SiteQuality
SIO_000300: 1.446e1

MQ
type: SiteQuality
SIO_000300: 5.974e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.66e-1

GenotypeQuality
all individuals: 278
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1302
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2300
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2453
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4251
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 695
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 623
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6625
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9698
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4517
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.075731497418244e-4
allele num: 9296
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47768
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.213e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.5e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.64e-1

FS
type: SiteQuality
SIO_000300: 6.413e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.181e1

VQSLOD
type: SiteQuality
SIO_000300: -4.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.38e-2

DP
type: SiteQuality
SIO_000300: 1.697468e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.08e-1

GenotypeQuality
all individuals: 163
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 504
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2434
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39315
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9294
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.354048964218456e-4
allele num: 8496
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9721
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4515
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6625
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47773
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.700045e6

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.237e0

FS
type: SiteQuality
SIO_000300: 8.523e0

MQRankSum
type: SiteQuality
SIO_000300: -5.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.615e-1

QD
type: SiteQuality
SIO_000300: 1.912e1

GenotypeQuality
all individuals: 7714
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4253
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2295
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1297
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2434
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39315
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4515
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6625
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9294
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.186465158143721e-5
allele num: 47773
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9721
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.615e-1

QD
type: SiteQuality
SIO_000300: 1.912e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -5.8e-2

FS
type: SiteQuality
SIO_000300: 8.523e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.237e0

DP
type: SiteQuality
SIO_000300: 1.700045e6

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.84e-1

GenotypeQuality
all individuals: 2437
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7754
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39445
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9295
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4516
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8495
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.184975936388365e-5
allele num: 47790
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6624
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.022704029453876e-4
allele num: 9778
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.25e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.13e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.163e0

DP
type: SiteQuality
SIO_000300: 1.702237e6

FS
type: SiteQuality
SIO_000300: 1.268e0

QD
type: SiteQuality
SIO_000300: 1.208e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.73e-2

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

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

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

GenotypeQuality
all individuals: 1275
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4242
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 499
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39778
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9286
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10021
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47853
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 629
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4509
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6623
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.791e0

MQ
type: SiteQuality
SIO_000300: 5.869e1

MQRankSum
type: SiteQuality
SIO_000300: -6.94e-1

QD
type: SiteQuality
SIO_000300: 3.44e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.58e-1

FS
type: SiteQuality
SIO_000300: 3.097e0

VQSLOD
type: SiteQuality
SIO_000300: -2.688e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.28e-1

DP
type: SiteQuality
SIO_000300: 1.711366e6

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

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

GenotypeQuality
all individuals: 332
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 2199
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4278
bin: 9.75e1
variant carriers: 47

GenotypeQuality
all individuals: 1046
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1262
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 326
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4495
num of homozygotes: 0

South Asian
type: Population
allele count: 59
allele frequency: 5.931436614054489e-3
allele num: 9947
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9256
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47738
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8472
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 7.987220447284345e-3
allele num: 626
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

FS
type: SiteQuality
SIO_000300: 5.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.275e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.878e-1

DP
type: SiteQuality
SIO_000300: 1.703615e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.329e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.75e-1

GenotypeQuality
all individuals: 523
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7408
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2196
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1256
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2360
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6609
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 625
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4492
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9249
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9935
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.096567918317714e-5
allele num: 47697
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.953e0

DP
type: SiteQuality
SIO_000300: 1.700532e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.085e0

FS
type: SiteQuality
SIO_000300: 9.211e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.599999999999999e-3

QD
type: SiteQuality
SIO_000300: 1.689e1

VQSLOD
type: SiteQuality
SIO_000300: -2.316e0

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7358
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2351
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2178
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1252
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1251
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9248
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8463
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.007962906965024e-4
allele num: 9921
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.098635886673662e-5
allele num: 47650
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4486
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.51285930408472e-4
allele num: 6610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.201e1

MQRankSum
type: SiteQuality
SIO_000300: -5.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.27e-1

FS
type: SiteQuality
SIO_000300: 6.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.688e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.72e-1

DP
type: SiteQuality
SIO_000300: 1.698121e6

GenotypeQuality
all individuals: 4228
bin: 9.75e1
variant carriers: 2

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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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7328
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2169
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4487
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.197271773347324e-5
allele num: 47650
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9247
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9918
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8462
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6607
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.745e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.53e-1

DP
type: SiteQuality
SIO_000300: 1.698225e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

MQ
type: SiteQuality
SIO_000300: 5.988e1

MQRankSum
type: SiteQuality
SIO_000300: 4.73e-1

QD
type: SiteQuality
SIO_000300: 1.208e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.47e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

GenotypeQuality
all individuals: 240
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 7.5e0
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GenotypeQuality
all individuals: 37698
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2099
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6581
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.086602194936434e-4
allele num: 9203
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8418
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9820
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47332
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4458
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -9.861e-1

FS
type: SiteQuality
SIO_000300: 4.605e0

BaseQRankSum
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SIO_000300: -2.229e0

QD
type: SiteQuality
SIO_000300: 1.929e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.61e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-2

DP
type: SiteQuality
SIO_000300: 1.677247e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.86e-1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 682
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6581
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9203
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.112735570016057e-5
allele num: 47332
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8418
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4458
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9820
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.929e1

DP
type: SiteQuality
SIO_000300: 1.677247e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.229e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.61e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.04e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.861e-1

FS
type: SiteQuality
SIO_000300: 4.605e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.86e-1

GenotypeQuality
all individuals: 2319
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 1
allele frequency: 1.520912547528517e-4
allele num: 6575
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9198
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8408
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4454
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47291
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.323e1

VQSLOD
type: SiteQuality
SIO_000300: -2.491e-1

DP
type: SiteQuality
SIO_000300: 1.67412e6

MQRankSum
type: SiteQuality
SIO_000300: -1.34e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.793e0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2201
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47040
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6561
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9162
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8374
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.029336078229542e-4
allele num: 9715
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4433
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.454e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.86e-1

QD
type: SiteQuality
SIO_000300: 2.092e1

DP
type: SiteQuality
SIO_000300: 1.660455e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.2e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.032e0

FS
type: SiteQuality
SIO_000300: 3.746e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.0e-3

GenotypeQuality
all individuals: 35426
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 427
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variant carriers: 0

GenotypeQuality
all individuals: 674
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9474
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6523
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.202356618973188e-4
allele num: 8317
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9093
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 603
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4381
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46468
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.3189e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.46e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.8e-1

QD
type: SiteQuality
SIO_000300: 1.139e1

MQRankSum
type: SiteQuality
SIO_000300: 4.79e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.641e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.79e-1

DP
type: SiteQuality
SIO_000300: 1.62859e6

GenotypeQuality
all individuals: 420
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4879
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variant carriers: 0

GenotypeQuality
all individuals: 11
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2120
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4368
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9095
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9464
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.065603923973023e-4
allele num: 6524
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8319
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46431
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.85e0

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.072e-1

QD
type: SiteQuality
SIO_000300: 1.371e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.031e0

DP
type: SiteQuality
SIO_000300: 1.624988e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.85e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

GenotypeQuality
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bin: 8.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 1712
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8913
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45147
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4263
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8201
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8961
num of homozygotes: 0

East Asian
type: Population
allele count: 23
allele frequency: 3.586464992983003e-3
allele num: 6413
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 589
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.498e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.16e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.89e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.55e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.51414e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.795e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

FS
type: SiteQuality
SIO_000300: 6.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.820000000000001e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 150
bin: 1.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 591
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6395
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.127777151234916e-4
allele num: 8867
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8175
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8897
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44987
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4247
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.098e-1

DP
type: SiteQuality
SIO_000300: 1.494841e6

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.833e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

FS
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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bin: 6.25e1
variant carriers: 0

Latino
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allele frequency: 0.0e0
allele num: 8877
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6384
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4251
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44882
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.225640397107489e-4
allele num: 8159
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 587
num of homozygotes: 0

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 3.033e1

DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
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allele frequency: 0.0e0
allele num: 8771
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
allele num: 8859
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East Asian
type: Population
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allele frequency: 1.099246231155779e-3
allele num: 6368
num of homozygotes: 0

African
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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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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 44767
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.604e0

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.76e-1

ReadPosRankSum
type: SiteQuality
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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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8028
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4093
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 43260
num of homozygotes: 0

East Asian
type: Population
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Other
type: Population
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allele frequency: 0.0e0
allele num: 568
num of homozygotes: 0

South Asian
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allele frequency: 1.232589670898558e-4
allele num: 8113
num of homozygotes: 0

DP
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1360
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
allele num: 6174
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African
type: Population
allele count: 1
allele frequency: 1.250156269533692e-4
allele num: 7999
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 2.319916483006612e-4
allele num: 8621
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42899
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4064
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.087e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
SIO_000300: 2.72e0

QD
type: SiteQuality
SIO_000300: 1.542e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-2

GenotypeQuality
all individuals: 952
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13541
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7983
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.341043168836033e-5
allele num: 42716
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6157
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4046
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7893
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.269e0

DP
type: SiteQuality
SIO_000300: 1.249798e6

VQSLOD
type: SiteQuality
SIO_000300: 9.409999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.078e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.203e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.387e0

GenotypeQuality
all individuals: 411
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 2330
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6029
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41630
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3961
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8451
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7505
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.266784899923993e-4
allele num: 7894
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.617e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 9.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

VQSLOD
type: SiteQuality
SIO_000300: 3.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.27e-1

DP
type: SiteQuality
SIO_000300: 1.211638e6

MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7856
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7354
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3928
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8382
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5981
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.844491812808837e-5
allele num: 41284
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 551
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.812e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.81e-1

DP
type: SiteQuality
SIO_000300: 1.206662e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

QD
type: SiteQuality
SIO_000300: 1.329e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.28e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 625
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3921
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5958
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 553
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7843
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41174
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.35795763172189e-4
allele num: 7364
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.275e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.20246e6

MQRankSum
type: SiteQuality
SIO_000300: 4.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

VQSLOD
type: SiteQuality
SIO_000300: -8.280999999999999e-1

QD
type: SiteQuality
SIO_000300: 9.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.16e-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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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7947
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5340
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.899391127863149e-5
allele num: 34490
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6652
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3885
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4001
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 451
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.79749e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.001e0

QD
type: SiteQuality
SIO_000300: 1.169e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.900000000000001e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.8e-2

FS
type: SiteQuality
SIO_000300: 5.902e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.78e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.55e-1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3888
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6675
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7975
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 451
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4014
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5357
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.891426919184618e-5
allele num: 34585
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.39e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.4e-3

DP
type: SiteQuality
SIO_000300: 9.8599e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.9e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3244
bin: 9.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8164
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3955
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6858
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.785670510891972e-5
allele num: 35898
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5538
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4245
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 475
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.406e1

VQSLOD
type: SiteQuality
SIO_000300: -1.983e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.533e0

DP
type: SiteQuality
SIO_000300: 1.088426e6

MQRankSum
type: SiteQuality
SIO_000300: -1.197e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.709e0

GenotypeQuality
all individuals: 33453
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 412
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GenotypeQuality
all individuals: 1679
bin: 8.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.26295541977823e-4
allele num: 4419
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8170
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9110
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6926
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44815
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.392666e6

VQSLOD
type: SiteQuality
SIO_000300: -2.242e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

MQ
type: SiteQuality
SIO_000300: 5.787e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.46e-1

QD
type: SiteQuality
SIO_000300: 2.975e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e-1

GenotypeQuality
all individuals: 5721
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variant carriers: 0

GenotypeQuality
all individuals: 5065
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GenotypeQuality
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GenotypeQuality
all individuals: 1809
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GenotypeQuality
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GenotypeQuality
all individuals: 767
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GenotypeQuality
all individuals: 698
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45860
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.090393632101189e-4
allele num: 9171
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8293
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4460
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.29e0

QD
type: SiteQuality
SIO_000300: 1.425e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.955e0

FS
type: SiteQuality
SIO_000300: 6.778e0

DP
type: SiteQuality
SIO_000300: 1.434498e6

MQRankSum
type: SiteQuality
SIO_000300: 1.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.889e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 239
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GenotypeQuality
all individuals: 913
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 598
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.40442414041837e-4
allele num: 8318
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9200
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46240
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7943
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.18e1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.451849e6

FS
type: SiteQuality
SIO_000300: 1.1643e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.36e0

MQRankSum
type: SiteQuality
SIO_000300: 5.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.24e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
all individuals: 1898
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GenotypeQuality
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GenotypeQuality
all individuals: 35584
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GenotypeQuality
all individuals: 925
bin: 9.25e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 601
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 3.445602549745887e-4
allele num: 46436
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9210
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4476
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.81e-1

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 6.92e-2

FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.973e1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.951e1

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.99e-1

GenotypeQuality
all individuals: 819
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variant carriers: 0

GenotypeQuality
all individuals: 524
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GenotypeQuality
all individuals: 46
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variant carriers: 0

GenotypeQuality
all individuals: 3442
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GenotypeQuality
all individuals: 612
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GenotypeQuality
all individuals: 1965
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3021
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8755
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4487
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8370
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9234
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.130651553244982e-5
allele num: 46934
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.317e-1

MQ
type: SiteQuality
SIO_000300: 5.861e1

QD
type: SiteQuality
SIO_000300: 1.066e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.653e0

FS
type: SiteQuality
SIO_000300: 1.7658e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

DP
type: SiteQuality
SIO_000300: 1.503412e6

GenotypeQuality
all individuals: 158
bin: 1.25e1
variant carriers: 45

GenotypeQuality
all individuals: 158
bin: 1.75e1
variant carriers: 41

GenotypeQuality
all individuals: 365
bin: 2.75e1
variant carriers: 60

GenotypeQuality
all individuals: 878
bin: 9.25e1
variant carriers: 86

GenotypeQuality
all individuals: 4451
bin: 9.75e1
variant carriers: 1678

GenotypeQuality
all individuals: 2309
bin: 7.25e1
variant carriers: 99

GenotypeQuality
all individuals: 634
bin: 5.25e1
variant carriers: 107

Other
type: Population
allele count: 26
allele frequency: 4.429301533219761e-2
allele num: 587
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 279
allele frequency: 6.506529850746269e-2
allele num: 4288
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 4.461298237787196e-4
allele num: 8966
num of homozygotes: 0

African
type: Population
allele count: 382
allele frequency: 4.836667510762218e-2
allele num: 7898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1116
allele frequency: 2.440197664757074e-2
allele num: 45734
num of homozygotes: 0

Latino
type: Population
allele count: 45
allele frequency: 4.88440247476392e-3
allele num: 9213
num of homozygotes: 0

East Asian
type: Population
allele count: 49
allele frequency: 7.493500535250038e-3
allele num: 6539
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.939e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.487e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.77e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.17e0

FS
type: SiteQuality
SIO_000300: 1.04319e2

DP
type: SiteQuality
SIO_000300: 1.647222e6

QD
type: SiteQuality
SIO_000300: 1.68e0

MQRankSum
type: SiteQuality
SIO_000300: -1.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.013e0

VQSLOD
type: SiteQuality
SIO_000300: -5.293e1

GenotypeQuality
all individuals: 6116
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5067
bin: 9.75e1
variant carriers: 19

GenotypeQuality
all individuals: 72
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 366
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2443
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 920
bin: 8.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 2
allele frequency: 4.444444444444445e-4
allele num: 4500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 5.929088106249259e-4
allele num: 8433
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.623376623376623e-3
allele num: 616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.960895036270964e-4
allele num: 47283
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9260
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9373
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.3515e1

MQRankSum
type: SiteQuality
SIO_000300: 1.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 1.633104e6

QD
type: SiteQuality
SIO_000300: 1.9e0

VQSLOD
type: SiteQuality
SIO_000300: -1.016e1

MQ
type: SiteQuality
SIO_000300: 5.946e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.714e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e-2

GenotypeQuality
all individuals: 2163
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35901
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2508
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6257
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5216
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 320
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1061
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 8.430281571404485e-5
allele num: 47448
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9271
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8461
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9455
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.697e0

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.93e-2

MQ
type: SiteQuality
SIO_000300: 5.948e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.2e-2

DP
type: SiteQuality
SIO_000300: 1.638651e6

QD
type: SiteQuality
SIO_000300: 1.457e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.51e-1

GenotypeQuality
all individuals: 235
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5239
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 956
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1077
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2576
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.077470100204719e-4
allele num: 9281
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8465
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9639
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 619
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47574
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.672e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.42e-1

DP
type: SiteQuality
SIO_000300: 1.648109e6

FS
type: SiteQuality
SIO_000300: 2.081e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.37e-2

MQ
type: SiteQuality
SIO_000300: 5.973e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.45e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.33e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.475e0

GenotypeQuality
all individuals: 36387
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5239
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 182
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3264
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6404
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2205
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.101988481103124e-5
allele num: 47574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8465
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4512
num of homozygotes: 0

East Asian
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: 619
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9639
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9281
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.33e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.475e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

MQRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

FS
type: SiteQuality
SIO_000300: 2.081e0

DP
type: SiteQuality
SIO_000300: 1.648109e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.37e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.45e-1

QD
type: SiteQuality
SIO_000300: 1.672e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.42e-1

GenotypeQuality
all individuals: 185
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3313
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36667
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2605
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5264
bin: 9.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47628
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.513546238837597e-4
allele num: 6607
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 621
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9282
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9733
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4511
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.14e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.05e0

MQRankSum
type: SiteQuality
SIO_000300: 3.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.42e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.683e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.846e0

DP
type: SiteQuality
SIO_000300: 1.651651e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.28e-1

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

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2677
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3385
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37396
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1102
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8491
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4515
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9299
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.091875156890637e-5
allele num: 47804
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 629
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9960
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6618
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.665619e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.59e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.012e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.52e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.396e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.82e-1

GenotypeQuality
all individuals: 2726
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6707
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5318
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2336
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.176055509820064e-4
allele num: 8503
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10072
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9306
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4518
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.959e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.08e-1

DP
type: SiteQuality
SIO_000300: 1.67417e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.52e0

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

GenotypeQuality
all individuals: 2741
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2352
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1115
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9306
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47934
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.980982567353407e-4
allele num: 10096
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6628
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4523
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.84e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.069e-1

QD
type: SiteQuality
SIO_000300: 3.029e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.676346e6

GenotypeQuality
all individuals: 6767
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5331
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2374
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37635
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6633
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47957
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10104
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 4.418912947414936e-4
allele num: 4526
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.073767851390529e-4
allele num: 9313
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.6e-1

QD
type: SiteQuality
SIO_000300: 1.59e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.879999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.44e-2

FS
type: SiteQuality
SIO_000300: 1.147e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

DP
type: SiteQuality
SIO_000300: 1.678774e6

GenotypeQuality
all individuals: 6765
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37611
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1120
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.507613447911955e-4
allele num: 6633
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9313
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47957
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4527
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.174674027957242e-4
allele num: 8513
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.979610016826685e-4
allele num: 10103
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 1.68e1

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

MQRankSum
type: SiteQuality
SIO_000300: 2.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.84e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.679172e6

FS
type: SiteQuality
SIO_000300: 1.4161e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.258e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.153e0

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

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1120
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6765
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2743
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5336
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2372
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4527
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8513
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9313
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6633
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.085201326188043e-5
allele num: 47957
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10103
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.258e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.84e-1

FS
type: SiteQuality
SIO_000300: 1.4161e1

QD
type: SiteQuality
SIO_000300: 1.68e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.153e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

DP
type: SiteQuality
SIO_000300: 1.679172e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

GenotypeQuality
all individuals: 93
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2379
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2749
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6736
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4527
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.085462242706096e-5
allele num: 47951
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9315
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.46e-1

MQ
type: SiteQuality
SIO_000300: 5.906e1

QD
type: SiteQuality
SIO_000300: 2.853e1

DP
type: SiteQuality
SIO_000300: 1.676691e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.62e-2

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

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6707
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1123
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2744
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3493
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2384
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.94431185361973e-5
allele num: 10056
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47945
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4526
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9316
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6637
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 629
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.120000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.39e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.993e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.71e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 4.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

DP
type: SiteQuality
SIO_000300: 1.675053e6

MQ
type: SiteQuality
SIO_000300: 5.878e1

GenotypeQuality
all individuals: 36774
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2748
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2383
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1019
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1124
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.085679723021733e-5
allele num: 47946
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9317
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6637
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10055
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.461e1

DP
type: SiteQuality
SIO_000300: 1.675219e6

VQSLOD
type: SiteQuality
SIO_000300: -8.740000000000001e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.96e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 1125
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2739
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2378
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9316
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.171794497403058e-5
allele num: 47941
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6637
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.968102073365231e-5
allele num: 10032
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 6.820000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.726e-1

DP
type: SiteQuality
SIO_000300: 1.672738e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.01e-1

QD
type: SiteQuality
SIO_000300: 3.201e1

FS
type: SiteQuality
SIO_000300: 1.684e0

MQRankSum
type: SiteQuality
SIO_000300: -2.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.047e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

GenotypeQuality
all individuals: 175
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3502
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9318
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.171881518564873e-5
allele num: 47940
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8509
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.977052778609199e-5
allele num: 10023
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.9e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.139e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.66e-1

FS
type: SiteQuality
SIO_000300: 6.42e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

QD
type: SiteQuality
SIO_000300: 2.047e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.11e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e0

DP
type: SiteQuality
SIO_000300: 1.671111e6

GenotypeQuality
all individuals: 6710
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2395
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1129
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9317
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.085984271678592e-5
allele num: 47939
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 6.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 1.670768e6

FS
type: SiteQuality
SIO_000300: 4.208e0

VQSLOD
type: SiteQuality
SIO_000300: -2.341e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.73e0

MQ
type: SiteQuality
SIO_000300: 5.886e1

QD
type: SiteQuality
SIO_000300: 8.26e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.15e-1

GenotypeQuality
all individuals: 147
bin: 5.25e1
variant carriers: 0

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