8-134128873-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128873
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128873
    reference: chr 8
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7775C>T
  hgvsp: ENSP00000220616.4:p.Pro2592Leu
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2885C>T
  hgvsp: ENSP00000441693.1:p.Pro962Leu
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3141C>T
  hgvsp: ENSP00000430523.1:p.Pro1048Leu
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*3988C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.122C>T
  hgvsp: ENSP00000430161.1:p.Pro41Leu
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7604C>T
  hgvsp: ENSP00000367100.1:p.Pro2535Leu
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2174C>T
  hgvsp: ENSP00000430430.1:p.Pro725Leu
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25038
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 944
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1517
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2240
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro2592Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

8-134128875-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128875
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128875
    reference: chr 8
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3143A>G
  hgvsp: ENSP00000430523.1:p.Ile1049Val
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*3990A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7606A>G
  hgvsp: ENSP00000367100.1:p.Ile2536Val
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2887A>G
  hgvsp: ENSP00000441693.1:p.Ile963Val
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2176A>G
  hgvsp: ENSP00000430430.1:p.Ile726Val
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.124A>G
  hgvsp: ENSP00000430161.1:p.Ile42Val
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7777A>G
  hgvsp: ENSP00000220616.4:p.Ile2593Val
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25042
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2240
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile2593Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/8-134128880-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128880
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128880
    reference: chr 8
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7782C>A
  hgvsp: ENST00000220616.4:c.7782C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3148C>A
  hgvsp: ENST00000519178.1:c.3148C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7611C>A
  hgvsp: ENST00000377869.1:c.7611C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.129C>A
  hgvsp: ENST00000521107.1:c.129C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2181C>A
  hgvsp: ENST00000519543.1:c.2181C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*3995C>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2892C>A
  hgvsp: ENST00000542445.1:c.2892C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13450
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3592
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8049
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1509
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34288
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2545
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ile2594Ile
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD

8-134128880-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128880
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128880
    reference: chr 8
allele count: 168
allele frequency: 1.383855024711697e-3
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.129C>T
  hgvsp: ENST00000521107.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7782C>T
  hgvsp: ENST00000220616.4:c.7782C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2892C>T
  hgvsp: ENST00000542445.1:c.2892C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*3995C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3148C>T
  hgvsp: ENST00000519178.1:c.3148C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2181C>T
  hgvsp: ENST00000519543.1:c.2181C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7611C>T
  hgvsp: ENST00000377869.1:c.7611C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8049
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 25028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13450
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 9.75e1
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 3592
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 4.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 8342
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2545
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1509
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile2594Ile
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

8-134128881-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128881
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128881
    reference: chr 8
allele count: 2
allele frequency: 1.647473599235572e-5
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7612G>A
  hgvsp: ENSP00000367100.1:p.Asp2538Asn
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.130G>A
  hgvsp: ENSP00000430161.1:p.Asp44Asn
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3149G>A
  hgvsp: ENSP00000430523.1:p.Asp1051Asn
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7783G>A
  hgvsp: ENSP00000220616.4:p.Asp2595Asn
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2182G>A
  hgvsp: ENSP00000430430.1:p.Asp728Asn
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2893G>A
  hgvsp: ENSP00000441693.1:p.Asp965Asn
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*3996G>A
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 939
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asp2595Asn
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS

8-134128881-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128881
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128881
    reference: chr 8
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7783G>T
  hgvsp: ENSP00000220616.4:p.Asp2595Tyr
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2893G>T
  hgvsp: ENSP00000441693.1:p.Asp965Tyr
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7612G>T
  hgvsp: ENSP00000367100.1:p.Asp2538Tyr
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.130G>T
  hgvsp: ENSP00000430161.1:p.Asp44Tyr
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*3996G>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3149G>T
  hgvsp: ENSP00000430523.1:p.Asp1051Tyr
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2182G>T
  hgvsp: ENSP00000430430.1:p.Asp728Tyr
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34379
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp2595Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

8-134128886-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128886
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128886
    reference: chr 8
allele count: 2
allele frequency: 1.647419317638919e-5
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.135G>A
  hgvsp: ENSP00000430161.1:p.Met45Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7788G>A
  hgvsp: ENSP00000220616.4:p.Met2596Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4001G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2898G>A
  hgvsp: ENSP00000441693.1:p.Met966Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7617G>A
  hgvsp: ENSP00000367100.1:p.Met2539Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3154G>A
  hgvsp: ENSP00000430523.1:p.Met1052Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2187G>A
  hgvsp: ENSP00000430430.1:p.Met729Ile
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25094
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34384
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1512
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10073
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 940
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Met2596Ile
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

8-134128890-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128890
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128890
    reference: chr 8
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2902A>G
  hgvsp: ENSP00000441693.1:p.Ser968Gly
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4005A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.139A>G
  hgvsp: ENSP00000430161.1:p.Ser47Gly
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2191A>G
  hgvsp: ENSP00000430430.1:p.Ser731Gly
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3158A>G
  hgvsp: ENSP00000430523.1:p.Ser1054Gly
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7621A>G
  hgvsp: ENSP00000367100.1:p.Ser2541Gly
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7792A>G
  hgvsp: ENSP00000220616.4:p.Ser2598Gly
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10072
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 940
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34394
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser2598Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

8-134128901-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128901
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128901
    reference: chr 8
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3169A>G
  hgvsp: ENST00000519178.1:c.3169A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7632A>G
  hgvsp: ENST00000377869.1:c.7632A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2202A>G
  hgvsp: ENST00000519543.1:c.2202A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4016A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2913A>G
  hgvsp: ENST00000542445.1:c.2913A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7803A>G
  hgvsp: ENST00000220616.4:c.7803A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.150A>G
  hgvsp: ENST00000521107.1:c.150A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13500
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25102
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 940
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10071
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala2601Ala
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS

http://identifiers.org/exac.variant/8-134128909-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128909
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128909
    reference: chr 8
allele count: 5
allele frequency: 4.118548294097296e-5
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7811C>A
  hgvsp: ENSP00000220616.4:p.Ala2604Asp
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7640C>A
  hgvsp: ENSP00000367100.1:p.Ala2547Asp
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2921C>A
  hgvsp: ENSP00000441693.1:p.Ala974Asp
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.158C>A
  hgvsp: ENSP00000430161.1:p.Ala53Asp
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2210C>A
  hgvsp: ENSP00000430430.1:p.Ala737Asp
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4024C>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3177C>A
  hgvsp: ENSP00000430523.1:p.Ala1060Asp
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2945
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10071
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34376
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8372
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1511
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala2604Asp
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum

8-134128911-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128911
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128911
    reference: chr 8
allele count: 4
allele frequency: 3.294838635277837e-5
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7813C>T
  hgvsp: ENSP00000220616.4:p.Arg2605Ter
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.160C>T
  hgvsp: ENSP00000430161.1:p.Arg54Ter
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7642C>T
  hgvsp: ENSP00000367100.1:p.Arg2548Ter
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2923C>T
  hgvsp: ENSP00000441693.1:p.Arg975Ter
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2212C>T
  hgvsp: ENSP00000430430.1:p.Arg738Ter
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3179C>T
  hgvsp: ENSP00000430523.1:p.Arg1061Ter
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4026C>T
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2946
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2242
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34377
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1510
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8371
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg2605Ter
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

8-134128912-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128912
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128912
    reference: chr 8
allele count: 3
allele frequency: 2.471169686985173e-5
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.161G>A
  hgvsp: ENSP00000430161.1:p.Arg54Gln
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2213G>A
  hgvsp: ENSP00000430430.1:p.Arg738Gln
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3180G>A
  hgvsp: ENSP00000430523.1:p.Arg1061Gln
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4027G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2924G>A
  hgvsp: ENSP00000441693.1:p.Arg975Gln
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7643G>A
  hgvsp: ENSP00000367100.1:p.Arg2548Gln
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7814G>A
  hgvsp: ENSP00000220616.4:p.Arg2605Gln
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8048
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2549
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10069
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg2605Gln
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS

8-134128915-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128915
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128914
    reference: chr 8
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7649delA
  hgvsp: ENSP00000367100.1:p.Asn2550ThrfsTer47
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2930delA
  hgvsp: ENSP00000441693.1:p.Asn977ThrfsTer47
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2219delA
  hgvsp: ENSP00000430430.1:p.Asn740ThrfsTer47
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3186delA
  hgvsp: ENSP00000430523.1:p.Asn1063ThrfsTer47
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4033delA
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7820delA
  hgvsp: ENSP00000220616.4:p.Asn2607ThrfsTer47
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.167delA
  hgvsp: ENSP00000430161.1:p.Asn56ThrfsTer59
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25100
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8048
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2549
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10067
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2242
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1509
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asn2607ThrfsTer47
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
reference allele: GA
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-134128916-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128916
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128916
    reference: chr 8
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3184A>C
  hgvsp: ENST00000519178.1:c.3184A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7647A>C
  hgvsp: ENST00000377869.1:c.7647A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.165A>C
  hgvsp: ENST00000521107.1:c.165A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7818A>C
  hgvsp: ENST00000220616.4:c.7818A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2928A>C
  hgvsp: ENST00000542445.1:c.2928A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2217A>C
  hgvsp: ENST00000519543.1:c.2217A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4031A>C
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25101
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8045
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1508
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34380
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2549
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly2606Gly
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: A
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

8-134128920-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128920
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128920
    reference: chr 8
allele count: 12
allele frequency: 9.884841595413434e-5
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3188G>A
  hgvsp: ENSP00000430523.1:p.Val1064Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.169G>A
  hgvsp: ENSP00000430161.1:p.Val57Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4035G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7651G>A
  hgvsp: ENSP00000367100.1:p.Val2551Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2932G>A
  hgvsp: ENSP00000441693.1:p.Val978Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7822G>A
  hgvsp: ENSP00000220616.4:p.Val2608Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2221G>A
  hgvsp: ENSP00000430430.1:p.Val741Ile
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13500
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25102
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8368
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val2608Ile
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

8-134128927-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128927
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128927
    reference: chr 8
allele count: 2
allele frequency: 1.647500741375333e-5
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7658T>A
  hgvsp: ENSP00000367100.1:p.Met2553Lys
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2939T>A
  hgvsp: ENSP00000441693.1:p.Met980Lys
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2228T>A
  hgvsp: ENSP00000430430.1:p.Met743Lys
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7829T>A
  hgvsp: ENSP00000220616.4:p.Met2610Lys
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.176T>A
  hgvsp: ENSP00000430161.1:p.Met59Lys
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3195T>A
  hgvsp: ENSP00000430523.1:p.Met1066Lys
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4042T>A
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25110
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10059
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2546
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2241
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Met2610Lys
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

8-134128930-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128930
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128930
    reference: chr 8
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2942A>G
  hgvsp: ENSP00000441693.1:p.Tyr981Cys
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3198A>G
  hgvsp: ENSP00000430523.1:p.Tyr1067Cys
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7661A>G
  hgvsp: ENSP00000367100.1:p.Tyr2554Cys
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4045A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7832A>G
  hgvsp: ENSP00000220616.4:p.Tyr2611Cys
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.179A>G
  hgvsp: ENSP00000430161.1:p.Tyr60Cys
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2231A>G
  hgvsp: ENSP00000430430.1:p.Tyr744Cys
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13500
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25111
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10057
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8369
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2546
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Tyr2611Cys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP

8-134128932-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128932
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128932
    reference: chr 8
allele count: 2
allele frequency: 1.647636465490254e-5
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2944C>G
  hgvsp: ENSP00000441693.1:p.His982Asp
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2233C>G
  hgvsp: ENSP00000430430.1:p.His745Asp
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.181C>G
  hgvsp: ENSP00000430161.1:p.His61Asp
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7663C>G
  hgvsp: ENSP00000367100.1:p.His2555Asp
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3200C>G
  hgvsp: ENSP00000430523.1:p.His1068Asp
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7834C>G
  hgvsp: ENSP00000220616.4:p.His2612Asp
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4047C>G
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25106
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8028
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1507
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 943
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
hgvs: p.His2612Asp
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

8-134128936-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128936
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128936
    reference: chr 8
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2237C>T
  hgvsp: ENSP00000430430.1:p.Ala746Val
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2948C>T
  hgvsp: ENSP00000441693.1:p.Ala983Val
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7667C>T
  hgvsp: ENSP00000367100.1:p.Ala2556Val
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7838C>T
  hgvsp: ENSP00000220616.4:p.Ala2613Val
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.185C>T
  hgvsp: ENSP00000430161.1:p.Ala62Val
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4051C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3204C>T
  hgvsp: ENSP00000430523.1:p.Ala1069Val
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8007
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25108
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10056
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala2613Val
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/8-134128938-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128938
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128938
    reference: chr 8
allele count: 26
allele frequency: 2.142068579149434e-4
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2950C>A
  hgvsp: ENSP00000441693.1:p.Pro984Thr
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7669C>A
  hgvsp: ENSP00000367100.1:p.Pro2557Thr
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4053C>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3206C>A
  hgvsp: ENSP00000430523.1:p.Pro1070Thr
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.187C>A
  hgvsp: ENSP00000430161.1:p.Pro63Thr
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7840C>A
  hgvsp: ENSP00000220616.4:p.Pro2614Thr
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2239C>A
  hgvsp: ENSP00000430430.1:p.Pro747Thr
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3594
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7998
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2951
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1818
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1502
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10060
  bin: 9.75e1
  variant carriers: 25
hgvs: p.Pro2614Thr
num of homozygotes: 1
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-134128945-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128945
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128945
    reference: chr 8
allele count: 3219
allele frequency: 2.65265760197775e-2
allele num: 121350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2246A>G
  hgvsp: ENSP00000430430.1:p.Asn749Ser
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7676A>G
  hgvsp: ENSP00000367100.1:p.Asn2559Ser
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7847A>G
  hgvsp: ENSP00000220616.4:p.Asn2616Ser
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3213A>G
  hgvsp: ENSP00000430523.1:p.Asn1072Ser
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.194A>G
  hgvsp: ENSP00000430161.1:p.Asn65Ser
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2957A>G
  hgvsp: ENSP00000441693.1:p.Asn986Ser
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4060A>G
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.25e1
  variant carriers: 208
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 4.25e1
  variant carriers: 123
genotype depth: GenotypeDepth
  all individuals: 24815
  bin: 2.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 8.75e1
  variant carriers: 156
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 4.75e1
  variant carriers: 155
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 9.75e1
  variant carriers: 683
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 201
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 5.25e1
  variant carriers: 184
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 3.75e1
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 7775
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 6.75e1
  variant carriers: 203
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.25e1
  variant carriers: 190
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 8.25e1
  variant carriers: 181
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.25e1
  variant carriers: 113
genotype depth: GenotypeDepth
  all individuals: 13186
  bin: 3.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 5.75e1
  variant carriers: 226
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8247
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn2616Ser
num of homozygotes: 423
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

8-134128945-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128945
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128945
    reference: chr 8
allele count: 192
allele frequency: 1.582200247218789e-3
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2957A>T
  hgvsp: ENSP00000441693.1:p.Asn986Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7676A>T
  hgvsp: ENSP00000367100.1:p.Asn2559Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.194A>T
  hgvsp: ENSP00000430161.1:p.Asn65Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3213A>T
  hgvsp: ENSP00000430523.1:p.Asn1072Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7847A>T
  hgvsp: ENSP00000220616.4:p.Asn2616Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2246A>T
  hgvsp: ENSP00000430430.1:p.Asn749Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4060A>T
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7775
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13186
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 8.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 8.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 24815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 9.75e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 6.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8247
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11012
  bin: 9.75e1
  variant carriers: 190
hgvs: p.Asn2616Ile
num of homozygotes: 2
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

8-134128949-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128949
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128949
    reference: chr 8
allele count: 2
allele frequency: 1.648478454386601e-5
allele num: 121324
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3217C>T
  hgvsp: ENST00000519178.1:c.3217C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7851C>T
  hgvsp: ENST00000220616.4:c.7851C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.198C>T
  hgvsp: ENST00000521107.1:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2250C>T
  hgvsp: ENST00000519543.1:c.2250C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2961C>T
  hgvsp: ENST00000542445.1:c.2961C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4064C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7680C>T
  hgvsp: ENST00000377869.1:c.7680C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13849
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3423
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26002
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8028
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 839
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35676
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8666
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Tyr2617Tyr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

8-134128954-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128954
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128954
    reference: chr 8
allele count: 1
allele frequency: 8.24551856066228e-6
allele num: 121278
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7856A>G
  hgvsp: ENSP00000220616.4:p.His2619Arg
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3222A>G
  hgvsp: ENSP00000430523.1:p.His1075Arg
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2966A>G
  hgvsp: ENSP00000441693.1:p.His989Arg
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2255A>G
  hgvsp: ENSP00000430430.1:p.His752Arg
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7685A>G
  hgvsp: ENSP00000367100.1:p.His2562Arg
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4069A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.203A>G
  hgvsp: ENSP00000430161.1:p.His68Arg
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7966
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2263
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35592
  bin: 6.25e1
  variant carriers: 0
hgvs: p.His2619Arg
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD

8-134128965-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128965
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128965
    reference: chr 8
allele count: 14
allele frequency: 1.157254331437641e-4
allele num: 120976
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2972+5G>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2261+5G>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4075+5G>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7691+5G>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.209+5G>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7862+5G>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3228+5G>C
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13680
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34971
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1431
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 3.25e1
  variant carriers: 0
hgvs: c.7862+5G>C
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-134128967-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128967
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128967
    reference: chr 8
allele count: 7
allele frequency: 5.78933439195448e-5
allele num: 120912
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3228+7C>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.209+7C>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2972+7C>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4075+7C>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2261+7C>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7691+7C>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7862+7C>A
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25675
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2960
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13655
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34874
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8495
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.75e1
  variant carriers: 0
hgvs: c.7862+7C>A
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD

8-134128967-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128967
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128967
    reference: chr 8
allele count: 13
allele frequency: 1.075162101362975e-4
allele num: 120912
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7691+7C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.209+7C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7862+7C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2972+7C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4075+7C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3228+7C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2261+7C>T
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2960
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25675
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13655
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8495
  bin: 9.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 8497
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1422
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
hgvs: c.7862+7C>T
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

8-134128968-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128968
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128968
    reference: chr 8
allele count: 8
allele frequency: 6.618571712224501e-5
allele num: 120872
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7862+8G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3228+8G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4075+8G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7691+8G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.209+8G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2972+8G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2261+8G>A
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2960
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7610
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8471
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 2232
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: c.7862+8G>A
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

8-134128976-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128976
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128976
    reference: chr 8
allele count: 3
allele frequency: 2.495051481228896e-5
allele num: 120238
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4075+16G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.209+16G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3228+16G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7862+16G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2261+16G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2972+16G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7691+16G>A
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24677
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2958
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7179
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1395
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2392
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7964
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP

8-134128994-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134128994
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134128994
    reference: chr 8
allele count: 5
allele frequency: 4.199069486201857e-5
allele num: 119074
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4075+34T>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2261+34T>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3228+34T>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7862+34T>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.209+34T>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7691+34T>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2972+34T>G
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6803
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8104
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8324
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17938
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1125
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4547
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4069
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5430
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 788
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1685
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1101
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2042
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2285
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

8-134129000-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134129000
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134129000
    reference: chr 8
allele count: 183
allele frequency: 1.545138302543146e-3
allele num: 118436
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.209+40C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7862+40C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2261+40C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4075+40C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2972+40C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3228+40C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7691+40C>T
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6837
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 7522
  bin: 2.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6906
  bin: 3.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 14886
  bin: 2.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 2958
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 3.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 11891
  bin: 1.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4761
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1959
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1892
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4615
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8580
  bin: 9.75e1
  variant carriers: 179
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 1
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

8-134129001-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134129001
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134129001
    reference: chr 8
allele count: 303
allele frequency: 2.563061462721413e-3
allele num: 118218
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4075+41G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7691+41G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3228+41G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.209+41G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2972+41G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7862+41G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2261+41G>A
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12505
  bin: 1.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 6589
  bin: 3.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 6883
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 4.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14293
  bin: 2.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 2960
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 7773
  bin: 2.25e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 3.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4895
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1492
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5154
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8660
  bin: 9.75e1
  variant carriers: 298
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 799
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1226
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4603
  bin: 6.75e1
  variant carriers: 1
num of homozygotes: 3
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ

8-134129006-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134129006
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134129006
    reference: chr 8
allele count: 6
allele frequency: 5.087505087505087e-5
allele num: 117936
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3228+46A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7691+46A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4075+46A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2261+46A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.209+46A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7862+46A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2972+46A>G
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6844
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12979
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11139
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11120
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1402
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4139
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4510
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2806
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5609
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3024
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

8-134129007-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134129007
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134129007
    reference: chr 8
allele count: 1
allele frequency: 8.512087163772557e-6
allele num: 117480
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2972+47T>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2261+47T>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7862+47T>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7691+47T>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4075+47T>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3228+47T>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.209+47T>A
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12386
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6757
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12966
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10128
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4055
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2810
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3299
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1842
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2321
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6356
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5646
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD

8-134129010-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134129010
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134129010
    reference: chr 8
allele count: 2
allele frequency: 1.721081527631964e-5
allele num: 116206
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4075+50G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7691+50G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.209+50G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3228+50G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2972+50G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2261+50G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7862+50G>A
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4891
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12880
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6715
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1190
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1863
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1313
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3119
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1783
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1206
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5467
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3501
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6583
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD

8-134144006-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144006
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144007
    reference: chr 8
allele count: 6
allele frequency: 4.952947003467063e-5
allele num: 121140
alternate allele: AG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3229-49dupG
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1707dupG
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4076-49dupG
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2262-49dupG
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7692-49dupG
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2973-49dupG
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7863-49dupG
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9672
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8630
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10290
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6884
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4075
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6095
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 781
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3312
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36770
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 2841
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3704
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

8-134144011-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144011
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144011
    reference: chr 8
allele count: 1
allele frequency: 8.252323028932645e-6
allele num: 121178
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1703A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7863-45A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3229-45A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7692-45A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4076-45A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2973-45A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2262-45A>G
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6861
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8636
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4340
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10326
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4077
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2528
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3290
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36793
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

8-134144017-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144017
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144017
    reference: chr 8
allele count: 3
allele frequency: 2.474512521033356e-5
allele num: 121236
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2262-39T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2973-39T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3229-39T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1697T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4076-39T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7692-39T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7863-39T>C
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9982
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8652
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4079
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10360
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2838
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

8-134144018-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144018
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144018
    reference: chr 8
allele count: 1
allele frequency: 8.24783082049421e-6
allele num: 121244
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7863-38C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2973-38C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4076-38C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1696C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2262-38C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3229-38C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7692-38C>T
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8658
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10011
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6108
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4255
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2052
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2844
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4146
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum

8-134144030-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144030
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144030
    reference: chr 8
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2973-26C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7863-26C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2262-26C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1684C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7692-26C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4076-26C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3229-26C>T
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6956
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10181
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4193
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36882
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3377
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2089
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

8-134144041-CCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144041
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144039
    reference: chr 8
allele count: 2
allele frequency: 1.64836976230508e-5
allele num: 121332
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1670_210-1669delCT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4076-12_*4076-11delCT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7692-12_7692-11delCT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2973-12_2973-11delCT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2262-12_2262-11delCT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3229-12_3229-11delCT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7863-12_7863-11delCT
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10230
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4759
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6137
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8702
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4081
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4502
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2909
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
reference allele: CCT
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

8-134144062-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144062
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144062
    reference: chr 8
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7869G>A
  hgvsp: ENST00000220616.4:c.7869G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1652G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4082G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7698G>A
  hgvsp: ENST00000377869.1:c.7698G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3235G>A
  hgvsp: ENST00000519178.1:c.3235G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2979G>A
  hgvsp: ENST00000542445.1:c.2979G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2268G>A
  hgvsp: ENST00000519543.1:c.2268G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10470
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4610
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8719
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10291
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2635
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4347
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2095
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3866
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu2623Glu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

8-134144071-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144071
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144071
    reference: chr 8
allele count: 6
allele frequency: 4.944212798918866e-5
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3244G>A
  hgvsp: ENST00000519178.1:c.3244G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2277G>A
  hgvsp: ENST00000519543.1:c.2277G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7707G>A
  hgvsp: ENST00000377869.1:c.7707G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7878G>A
  hgvsp: ENST00000220616.4:c.7878G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2988G>A
  hgvsp: ENST00000542445.1:c.2988G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1643G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4091G>A
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4601
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7052
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10277
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10457
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6149
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8713
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2098
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3872
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3416
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala2626Ala
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

8-134144075-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144075
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144075
    reference: chr 8
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2281G>A
  hgvsp: ENSP00000430430.1:p.Val761Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4095G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2992G>A
  hgvsp: ENSP00000441693.1:p.Val998Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7882G>A
  hgvsp: ENSP00000220616.4:p.Val2628Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7711G>A
  hgvsp: ENSP00000367100.1:p.Val2571Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3248G>A
  hgvsp: ENSP00000430523.1:p.Val1084Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1639G>A
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4634
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10457
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10270
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4084
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8716
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2097
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4207
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2638
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val2628Ile
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

8-134144076-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144076
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144076
    reference: chr 8
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4096T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3249T>C
  hgvsp: ENSP00000430523.1:p.Val1084Ala
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2993T>C
  hgvsp: ENSP00000441693.1:p.Val998Ala
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7712T>C
  hgvsp: ENSP00000367100.1:p.Val2571Ala
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1638T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7883T>C
  hgvsp: ENSP00000220616.4:p.Val2628Ala
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2282T>C
  hgvsp: ENSP00000430430.1:p.Val761Ala
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10459
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4084
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2919
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4447
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4206
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val2628Ala
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

8-134144082-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144082
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144082
    reference: chr 8
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4102T>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7889T>A
  hgvsp: ENSP00000220616.4:p.Phe2630Tyr
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.2999T>A
  hgvsp: ENSP00000441693.1:p.Phe1000Tyr
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1632T>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2288T>A
  hgvsp: ENSP00000430430.1:p.Phe763Tyr
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3255T>A
  hgvsp: ENSP00000430523.1:p.Phe1086Tyr
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7718T>A
  hgvsp: ENSP00000367100.1:p.Phe2573Tyr
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7043
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8716
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10462
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4458
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2101
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Phe2630Tyr
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

8-134144098-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144098
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144098
    reference: chr 8
allele count: 3
allele frequency: 2.471291826614165e-5
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7734C>T
  hgvsp: ENST00000377869.1:c.7734C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4118C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1616C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3015C>T
  hgvsp: ENST00000542445.1:c.3015C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3271C>T
  hgvsp: ENST00000519178.1:c.3271C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7905C>T
  hgvsp: ENST00000220616.4:c.7905C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2304C>T
  hgvsp: ENST00000519543.1:c.2304C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2540
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10289
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10468
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3441
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4212
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro2635Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

8-134144105-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144105
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144105
    reference: chr 8
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4125C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1609C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3022C>T
  hgvsp: ENSP00000441693.1:p.Pro1008Ser
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3278C>T
  hgvsp: ENSP00000430523.1:p.Pro1094Ser
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7912C>T
  hgvsp: ENSP00000220616.4:p.Pro2638Ser
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7741C>T
  hgvsp: ENSP00000367100.1:p.Pro2581Ser
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2311C>T
  hgvsp: ENSP00000430430.1:p.Pro771Ser
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8731
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4567
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6161
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10471
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10303
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro2638Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/8-134144113-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144113
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144113
    reference: chr 8
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2319C>A
  hgvsp: ENSP00000430430.1:p.Tyr773Ter
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3030C>A
  hgvsp: ENSP00000441693.1:p.Tyr1010Ter
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7749C>A
  hgvsp: ENSP00000367100.1:p.Tyr2583Ter
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7920C>A
  hgvsp: ENSP00000220616.4:p.Tyr2640Ter
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4133C>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3286C>A
  hgvsp: ENSP00000430523.1:p.Tyr1096Ter
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1601C>A
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3511
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15721
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3554
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2872
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1417
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52859
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Tyr2640Ter
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

8-134144113-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144113
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144113
    reference: chr 8
allele count: 52612
allele frequency: 4.335415396278656e-1
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4133C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3030C>T
  hgvsp: ENST00000542445.1:c.3030C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3286C>T
  hgvsp: ENST00000519178.1:c.3286C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7920C>T
  hgvsp: ENST00000220616.4:c.7920C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7749C>T
  hgvsp: ENST00000377869.1:c.7749C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1601C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2319C>T
  hgvsp: ENST00000519543.1:c.2319C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 4.25e1
  variant carriers: 401
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 7.25e1
  variant carriers: 3149
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 2.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 2872
  bin: 9.25e1
  variant carriers: 2777
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 3.75e1
  variant carriers: 234
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 7.75e1
  variant carriers: 3446
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 5.25e1
  variant carriers: 1063
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 5.75e1
  variant carriers: 1559
genotype depth: GenotypeDepth
  all individuals: 3511
  bin: 3.25e1
  variant carriers: 126
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 6.25e1
  variant carriers: 2181
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 2.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3554
  bin: 8.25e1
  variant carriers: 3405
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 6.75e1
  variant carriers: 2657
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 8.75e1
  variant carriers: 3108
genotype depth: GenotypeDepth
  all individuals: 15721
  bin: 9.75e1
  variant carriers: 15413
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 4.75e1
  variant carriers: 709
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1096
  bin: 7.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 1
hgvs: p.Tyr2640Tyr
num of homozygotes: 12299
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

8-134144114-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144114
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144114
    reference: chr 8
allele count: 3
allele frequency: 2.471169686985173e-5
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3031G>A
  hgvsp: ENSP00000441693.1:p.Glu1011Lys
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7921G>A
  hgvsp: ENSP00000220616.4:p.Glu2641Lys
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4134G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3287G>A
  hgvsp: ENSP00000430523.1:p.Glu1097Lys
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7750G>A
  hgvsp: ENSP00000367100.1:p.Glu2584Lys
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1600G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2320G>A
  hgvsp: ENSP00000430430.1:p.Glu774Lys
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8852
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3990
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3620
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4147
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1610
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1131
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1677
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1907
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Glu2641Lys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

8-134144114-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144114
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144114
    reference: chr 8
allele count: 5
allele frequency: 4.118616144975288e-5
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7921G>C
  hgvsp: ENSP00000220616.4:p.Glu2641Gln
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3287G>C
  hgvsp: ENSP00000430523.1:p.Glu1097Gln
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1600G>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4134G>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3031G>C
  hgvsp: ENSP00000441693.1:p.Glu1011Gln
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2320G>C
  hgvsp: ENSP00000430430.1:p.Glu774Gln
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7750G>C
  hgvsp: ENSP00000367100.1:p.Glu2584Gln
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4147
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3620
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3990
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8852
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1362
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1126
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1677
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu2641Gln
num of homozygotes: 1
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD

8-134144118-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144118
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144118
    reference: chr 8
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7925G>A
  hgvsp: ENSP00000220616.4:p.Gly2642Glu
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3291G>A
  hgvsp: ENSP00000430523.1:p.Gly1098Glu
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3035G>A
  hgvsp: ENSP00000441693.1:p.Gly1012Glu
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1596G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4138G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7754G>A
  hgvsp: ENSP00000367100.1:p.Gly2585Glu
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2324G>A
  hgvsp: ENSP00000430430.1:p.Gly775Glu
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3620
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3075
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3868
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4147
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3989
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8849
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1128
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1909
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly2642Glu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

8-134144119-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144119
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144119
    reference: chr 8
allele count: 3
allele frequency: 2.471210398853358e-5
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3036G>T
  hgvsp: ENST00000542445.1:c.3036G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7755G>T
  hgvsp: ENST00000377869.1:c.7755G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7926G>T
  hgvsp: ENST00000220616.4:c.7926G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1595G>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2325G>T
  hgvsp: ENST00000519543.1:c.2325G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3292G>T
  hgvsp: ENST00000519178.1:c.3292G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4139G>T
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3919
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3620
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4147
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3988
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8851
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1363
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 858
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1610
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly2642Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

8-134144130-TGGA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144130
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144127
    reference: chr 8
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7771_7773delGAG
  hgvsp: ENSP00000367100.1:p.Glu2591del
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4155_*4157delGAG
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3308_3310delGAG
  hgvsp: ENSP00000430523.1:p.Glu1104del
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3052_3054delGAG
  hgvsp: ENSP00000441693.1:p.Glu1018del
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2341_2343delGAG
  hgvsp: ENSP00000430430.1:p.Glu781del
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1579_210-1577delGAG
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7942_7944delGAG
  hgvsp: ENSP00000220616.4:p.Glu2648del
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 4148
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3868
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3919
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3985
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8851
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3620
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 858
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1134
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1359
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu2648del
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: TGGA
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

8-134144132-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144132
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144132
    reference: chr 8
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3305G>T
  hgvsp: ENSP00000430523.1:p.Glu1103Ter
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7768G>T
  hgvsp: ENSP00000367100.1:p.Glu2590Ter
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3049G>T
  hgvsp: ENSP00000441693.1:p.Glu1017Ter
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1582G>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7939G>T
  hgvsp: ENSP00000220616.4:p.Glu2647Ter
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2338G>T
  hgvsp: ENSP00000430430.1:p.Glu780Ter
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4152G>T
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4148
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3987
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8852
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3619
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1361
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu2647Ter
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

8-134144136-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144136
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144136
    reference: chr 8
allele count: 2
allele frequency: 1.647446457990115e-5
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1578A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7772A>G
  hgvsp: ENSP00000367100.1:p.Glu2591Gly
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3053A>G
  hgvsp: ENSP00000441693.1:p.Glu1018Gly
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3309A>G
  hgvsp: ENSP00000430523.1:p.Glu1104Gly
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2342A>G
  hgvsp: ENSP00000430430.1:p.Glu781Gly
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7943A>G
  hgvsp: ENSP00000220616.4:p.Glu2648Gly
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4156A>G
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3987
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8852
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1690
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1359
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu2648Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

8-134144140-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144140
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144140
    reference: chr 8
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3057G>A
  hgvsp: ENST00000542445.1:c.3057G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3313G>A
  hgvsp: ENST00000519178.1:c.3313G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7947G>A
  hgvsp: ENST00000220616.4:c.7947G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1574G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7776G>A
  hgvsp: ENST00000377869.1:c.7776G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2346G>A
  hgvsp: ENST00000519543.1:c.2346G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4160G>A
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8851
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3987
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1612
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50994
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Lys2649Lys
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

8-134144148-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144148
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144148
    reference: chr 8
allele count: 2
allele frequency: 1.647310765175851e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7955C>T
  hgvsp: ENSP00000220616.4:p.Ser2652Leu
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3321C>T
  hgvsp: ENSP00000430523.1:p.Ser1108Leu
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3065C>T
  hgvsp: ENSP00000441693.1:p.Ser1022Leu
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1566C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2354C>T
  hgvsp: ENSP00000430430.1:p.Ser785Leu
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4168C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7784C>T
  hgvsp: ENSP00000367100.1:p.Ser2595Leu
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3987
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8852
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1612
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser2652Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

8-134144149-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144149
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144149
    reference: chr 8
allele count: 7
allele frequency: 5.765682656826568e-5
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3066G>A
  hgvsp: ENST00000542445.1:c.3066G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3322G>A
  hgvsp: ENST00000519178.1:c.3322G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2355G>A
  hgvsp: ENST00000519543.1:c.2355G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7785G>A
  hgvsp: ENST00000377869.1:c.7785G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7956G>A
  hgvsp: ENST00000220616.4:c.7956G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4169G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1565G>A
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3988
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4150
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8852
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1906
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1696
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser2652Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

8-134144154-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144154
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144154
    reference: chr 8
allele count: 4
allele frequency: 3.294621530351701e-5
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7961A>G
  hgvsp: ENSP00000220616.4:p.Lys2654Arg
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4174A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7790A>G
  hgvsp: ENSP00000367100.1:p.Lys2597Arg
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3071A>G
  hgvsp: ENSP00000441693.1:p.Lys1024Arg
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1560A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3327A>G
  hgvsp: ENSP00000430523.1:p.Lys1110Arg
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2360A>G
  hgvsp: ENSP00000430430.1:p.Lys787Arg
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3919
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3619
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8851
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3988
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1135
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50995
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1612
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Lys2654Arg
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

8-134144161-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144161
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144161
    reference: chr 8
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2367G>A
  hgvsp: ENSP00000430430.1:p.Met789Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3078G>A
  hgvsp: ENSP00000441693.1:p.Met1026Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3334G>A
  hgvsp: ENSP00000430523.1:p.Met1112Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7968G>A
  hgvsp: ENSP00000220616.4:p.Met2656Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4181G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1553G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7797G>A
  hgvsp: ENSP00000367100.1:p.Met2599Ile
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8851
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3988
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3919
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3619
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1361
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1906
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50995
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Met2656Ile
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP

8-134144163-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144163
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144163
    reference: chr 8
allele count: 7
allele frequency: 5.765587678115476e-5
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3080A>G
  hgvsp: ENSP00000441693.1:p.Gln1027Arg
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2369A>G
  hgvsp: ENSP00000430430.1:p.Gln790Arg
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7970A>G
  hgvsp: ENSP00000220616.4:p.Gln2657Arg
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3336A>G
  hgvsp: ENSP00000430523.1:p.Gln1113Arg
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4183A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1551A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7799A>G
  hgvsp: ENSP00000367100.1:p.Gln2600Arg
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8854
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2560
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3986
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1135
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1361
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln2657Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD

8-134144167-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144167
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144167
    reference: chr 8
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2373C>T
  hgvsp: ENST00000519543.1:c.2373C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1547C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3084C>T
  hgvsp: ENST00000542445.1:c.3084C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4187C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3340C>T
  hgvsp: ENST00000519178.1:c.3340C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7803C>T
  hgvsp: ENST00000377869.1:c.7803C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7974C>T
  hgvsp: ENST00000220616.4:c.7974C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8852
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3986
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4150
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1613
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Tyr2658Tyr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

8-134144172-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144172
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144172
    reference: chr 8
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3345C>G
  hgvsp: ENSP00000430523.1:p.Ser1116Cys
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7979C>G
  hgvsp: ENSP00000220616.4:p.Ser2660Cys
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2378C>G
  hgvsp: ENSP00000430430.1:p.Ser793Cys
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3089C>G
  hgvsp: ENSP00000441693.1:p.Ser1030Cys
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7808C>G
  hgvsp: ENSP00000367100.1:p.Ser2603Cys
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1542C>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4192C>G
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3986
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4150
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8853
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1134
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1133
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser2660Cys
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum

8-134144176-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144176
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144176
    reference: chr 8
allele count: 3
allele frequency: 2.470966147763776e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2382C>T
  hgvsp: ENST00000519543.1:c.2382C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3093C>T
  hgvsp: ENST00000542445.1:c.3093C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4196C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7983C>T
  hgvsp: ENST00000220616.4:c.7983C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7812C>T
  hgvsp: ENST00000377869.1:c.7812C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1538C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3349C>T
  hgvsp: ENST00000519178.1:c.3349C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8854
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3987
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1696
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.His2661His
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

8-134144188-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144188
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144188
    reference: chr 8
allele count: 3
allele frequency: 2.470966147763776e-5
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2394A>G
  hgvsp: ENST00000519543.1:c.2394A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3361A>G
  hgvsp: ENST00000519178.1:c.3361A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7995A>G
  hgvsp: ENST00000220616.4:c.7995A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1526A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4208A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3105A>G
  hgvsp: ENST00000542445.1:c.3105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7824A>G
  hgvsp: ENST00000377869.1:c.7824A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4148
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3987
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8856
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4167
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1359
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1695
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1133
  bin: 8.75e1
  variant carriers: 0
hgvs: c.7995A>G
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

8-134144188-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144188
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144188
    reference: chr 8
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2394A>T
  hgvsp: ENST00000519543.1:c.2394A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1526A>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3105A>T
  hgvsp: ENST00000542445.1:c.3105A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7824A>T
  hgvsp: ENST00000377869.1:c.7824A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4208A>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3361A>T
  hgvsp: ENST00000519178.1:c.3361A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7995A>T
  hgvsp: ENST00000220616.4:c.7995A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4167
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8856
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3987
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4148
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1133
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
hgvs: c.7995A>T
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

8-134144190-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144190
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144190
    reference: chr 8
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7997G>A
  hgvsp: ENSP00000220616.4:p.Gly2666Glu
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7826G>A
  hgvsp: ENSP00000367100.1:p.Gly2609Glu
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3107G>A
  hgvsp: ENSP00000441693.1:p.Gly1036Glu
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1524G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3363G>A
  hgvsp: ENSP00000430523.1:p.Gly1122Glu
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2396G>A
  hgvsp: ENSP00000430430.1:p.Gly799Glu
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4210G>A
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4167
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3987
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8855
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4148
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1134
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1359
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 863
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly2666Glu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

8-134144206-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144206
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144206
    reference: chr 8
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1508T>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3363+16T>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4210+16T>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7826+16T>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2396+16T>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7997+16T>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3107+16T>A
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4167
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8856
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3987
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4148
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1691
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50996
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1359
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1132
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

8-134144208-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144208
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144208
    reference: chr 8
allele count: 4
allele frequency: 3.294621530351701e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2396+18G>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3363+18G>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4210+18G>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7997+18G>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3107+18G>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7826+18G>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1506G>T
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3866
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8858
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3987
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4168
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4148
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1132
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1902
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50996
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

8-134144225-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134144225
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 134144225
    reference: chr 8
allele count: 8
allele frequency: 6.589351607801793e-5
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.7826+35T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.2396+35T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.7997+35T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.3107+35T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000428628
  ensembl transcript: ENST00000523756
  gene symbol: TG
  hgvsc: ENST00000523756.1:c.*4210+35T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430161
  ensembl transcript: ENST00000521107
  gene symbol: TG
  hgvsc: ENST00000521107.1:c.210-1489T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.3363+35T>C
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4148
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4167
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3619
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4272
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3987
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8856
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 8348
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 34283
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2553
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10168
bin: 9.75e1
variant carriers: 1

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

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

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 2.205508e6

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

FS
type: SiteQuality
SIO_000300: 8.303000000000001e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.87e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.356e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.654e-1

QD
type: SiteQuality
SIO_000300: 9.26e0

GenotypeQuality
all individuals: 2554
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 944
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10167
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1517
bin: 8.25e1
variant carriers: 0

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

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.471e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.11e-1

DP
type: SiteQuality
SIO_000300: 2.20544e6

FS
type: SiteQuality
SIO_000300: 9.07e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.41e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.76e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

QD
type: SiteQuality
SIO_000300: 2.082e1

GenotypeQuality
all individuals: 10222
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2236
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 935
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 602
bin: 8.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 5.69e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.81e-1

DP
type: SiteQuality
SIO_000300: 2.216419e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.04e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.201e1

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 168

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 935
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 13
allele frequency: 1.122819139747797e-3
allele num: 11578
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 128
allele frequency: 1.91812024216268e-3
allele num: 66732
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.843936190659235e-4
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 7.559721802237678e-4
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 18
allele frequency: 1.090116279069767e-3
allele num: 16512
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.216419e6

MQRankSum
type: SiteQuality
SIO_000300: 2.81e-1

QD
type: SiteQuality
SIO_000300: 1.201e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.21e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

MQ
type: SiteQuality
SIO_000300: 5.966e1

GenotypeQuality
all individuals: 1512
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8374
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10075
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 34379
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2551
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2240
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.20412e6

MQ
type: SiteQuality
SIO_000300: 5.947e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.253e1

MQRankSum
type: SiteQuality
SIO_000300: 8.45e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 2240
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2551
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10075
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 939
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1512
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.20412e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

QD
type: SiteQuality
SIO_000300: 1.253e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.26e-1

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

GenotypeQuality
all individuals: 2242
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2551
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 2.203955e6

FS
type: SiteQuality
SIO_000300: 2.025e0

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.72e-1

QD
type: SiteQuality
SIO_000300: 1.292e1

VQSLOD
type: SiteQuality
SIO_000300: 7.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.81e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 2242
bin: 7.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.69e-1

QD
type: SiteQuality
SIO_000300: 1.036e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.102e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.708e0

DP
type: SiteQuality
SIO_000300: 2.203867e6

MQRankSum
type: SiteQuality
SIO_000300: -4.03e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.6e-1

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

GenotypeQuality
all individuals: 1511
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 34391
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 8372
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variant carriers: 0

GenotypeQuality
all individuals: 603
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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European (Finnish)
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South Asian
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African
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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ClippingRankSum
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DP
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MQ
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VQSLOD
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InbreedingCoeff
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MQRankSum
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QD
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ReadPosRankSum
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BaseQRankSum
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Latino
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Other
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European (Non-Finnish)
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South Asian
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European (Finnish)
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BaseQRankSum
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MQ
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VQSLOD
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QD
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FS
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InbreedingCoeff
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ReadPosRankSum
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DP
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ClippingRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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European (Non-Finnish)
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East Asian
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African
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Other
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European (Finnish)
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ReadPosRankSum
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QD
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VQSLOD
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MQ
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MQRankSum
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DP
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FS
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.498621268433042e-5
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Other
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African
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East Asian
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South Asian
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European (Finnish)
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DP
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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QD
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MQ
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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European (Non-Finnish)
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East Asian
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European (Finnish)
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Latino
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FS
type: SiteQuality
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VQSLOD
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DP
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InbreedingCoeff
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MQ
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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European (Finnish)
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Latino
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East Asian
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South Asian
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Other
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DP
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MQ
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InbreedingCoeff
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ClippingRankSum
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FS
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MQRankSum
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ReadPosRankSum
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VQSLOD
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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European (Non-Finnish)
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African
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Other
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Latino
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South Asian
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DP
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FS
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MQRankSum
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BaseQRankSum
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QD
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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Latino
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East Asian
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African
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South Asian
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FS
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MQ
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MQRankSum
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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African
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European (Finnish)
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South Asian
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East Asian
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FS
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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VQSLOD
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QD
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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European (Non-Finnish)
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Other
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East Asian
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Latino
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allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.937e1

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

FS
type: SiteQuality
SIO_000300: 5.96e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.35e-1

DP
type: SiteQuality
SIO_000300: 2.203386e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.597e0

VQSLOD
type: SiteQuality
SIO_000300: -2.225e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.8e-2

QD
type: SiteQuality
SIO_000300: 2.456e1

GenotypeQuality
all individuals: 8370
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 944
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2544
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34351
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2241
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.949e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.75e-1

DP
type: SiteQuality
SIO_000300: 2.202991e6

QD
type: SiteQuality
SIO_000300: 1.337e1

VQSLOD
type: SiteQuality
SIO_000300: -8.627e-1

FS
type: SiteQuality
SIO_000300: 1.771e0

MQRankSum
type: SiteQuality
SIO_000300: -1.873e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.916e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

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

GenotypeQuality
all individuals: 599
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2546
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2238
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 944
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34358
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8370
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 6
allele frequency: 5.183137525915688e-4
allele num: 11576
num of homozygotes: 0

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

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

African
type: Population
allele count: 20
allele frequency: 1.921968095329617e-3
allele num: 10406
num of homozygotes: 1

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.19e-2

DP
type: SiteQuality
SIO_000300: 2.204254e6

QD
type: SiteQuality
SIO_000300: 1.387e1

FS
type: SiteQuality
SIO_000300: 5.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.807e0

MQRankSum
type: SiteQuality
SIO_000300: 1.88e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.56e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e-1

GenotypeQuality
all individuals: 2157
bin: 7.25e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1351
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 11012
bin: 9.75e1
variant carriers: 2785

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 34091
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2384
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 82
allele frequency: 1.229164168365511e-3
allele num: 66712
num of homozygotes: 0

African
type: Population
allele count: 2924
allele frequency: 2.810997885022111e-1
allele num: 10402
num of homozygotes: 418

South Asian
type: Population
allele count: 10
allele frequency: 6.05766900896535e-4
allele num: 16508
num of homozygotes: 0

Latino
type: Population
allele count: 191
allele frequency: 1.650535776011061e-2
allele num: 11572
num of homozygotes: 5

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 11
allele frequency: 1.211453744493392e-2
allele num: 908
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.721e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.38e0

FS
type: SiteQuality
SIO_000300: 1.276e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.248e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.06e0

DP
type: SiteQuality
SIO_000300: 2.313308e6

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2157
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34091
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2384
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1351
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.42306760358614e-4
allele num: 16508
num of homozygotes: 0

East Asian
type: Population
allele count: 178
allele frequency: 2.061616863562659e-2
allele num: 8634
num of homozygotes: 2

Other
type: Population
allele count: 5
allele frequency: 5.506607929515419e-3
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.494903465643362e-5
allele num: 66712
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.248e-1

DP
type: SiteQuality
SIO_000300: 2.313308e6

VQSLOD
type: SiteQuality
SIO_000300: 9.06e0

FS
type: SiteQuality
SIO_000300: 1.276e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.38e0

QD
type: SiteQuality
SIO_000300: 1.721e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.79e-1

GenotypeQuality
all individuals: 8511
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1447
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2272
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2525
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 533
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.212121212121212e-4
allele num: 16500
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.217e1

VQSLOD
type: SiteQuality
SIO_000300: -2.833e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.59e-1

DP
type: SiteQuality
SIO_000300: 2.171508e6

FS
type: SiteQuality
SIO_000300: 6.343e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.52e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.77e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1444
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 838
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 185
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8635
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8508
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2520
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499925003749813e-5
allele num: 66670
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.38e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.216e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.78e-1

DP
type: SiteQuality
SIO_000300: 2.169872e6

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

FS
type: SiteQuality
SIO_000300: 2.265e0

QD
type: SiteQuality
SIO_000300: 2.208e1

GenotypeQuality
all individuals: 2494
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8512
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8502
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 63
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2246
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.493246390312063e-4
allele num: 8588
num of homozygotes: 0

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

South Asian
type: Population
allele count: 11
allele frequency: 6.677188296709967e-4
allele num: 16474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66526
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.632e0

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.402e1

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.850000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.159936e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.73e-1

GenotypeQuality
all individuals: 2243
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 527
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2478
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1422
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8497
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

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

Latino
type: Population
allele count: 5
allele frequency: 4.346314325452017e-4
allele num: 11504
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.008242584682029e-5
allele num: 66484
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.37e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.36e0

MQRankSum
type: SiteQuality
SIO_000300: -1.04e-1

FS
type: SiteQuality
SIO_000300: 1.143e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.157165e6

QD
type: SiteQuality
SIO_000300: 1.394e1

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

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

GenotypeQuality
all individuals: 527
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 694
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2243
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2478
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34874
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 3.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.214181641573579e-4
allele num: 16472
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.008242584682029e-5
allele num: 66484
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 7.82336578581363e-4
allele num: 11504
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.157165e6

MQRankSum
type: SiteQuality
SIO_000300: -1.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.37e0

FS
type: SiteQuality
SIO_000300: 1.143e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.36e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 1.394e1

GenotypeQuality
all individuals: 2467
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 820
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1417
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 34805
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8492
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 2.25e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66470
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 4.857906242409522e-4
allele num: 16468
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.71e-1

MQ
type: SiteQuality
SIO_000300: 5.99e1

DP
type: SiteQuality
SIO_000300: 2.155244e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.03e-1

FS
type: SiteQuality
SIO_000300: 3.096e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.196e0

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.161e1

GenotypeQuality
all individuals: 2134
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 634
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 810
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8449
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 33014
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1921
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.536793394428818e-5
allele num: 66126
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11434
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10290
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.72e-1

FS
type: SiteQuality
SIO_000300: 1.736e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.975e0

MQRankSum
type: SiteQuality
SIO_000300: 4.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.09e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

QD
type: SiteQuality
SIO_000300: 1.332e1

DP
type: SiteQuality
SIO_000300: 2.117727e6

GenotypeQuality
all individuals: 28
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 793
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 947
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3163
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 125
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1284
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8430
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 22119
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 5
allele frequency: 4.900039200313603e-4
allele num: 10204
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11326
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8294
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65474
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16368
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.8e-2

QD
type: SiteQuality
SIO_000300: 1.525e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.47e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.81e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.84e-1

DP
type: SiteQuality
SIO_000300: 1.935733e6

MQ
type: SiteQuality
SIO_000300: 5.938e1

GenotypeQuality
all individuals: 2586
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1562
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4672
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 774
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18722
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1887
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1258
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5000
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.218620521569583e-4
allele num: 8206
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.623921085080148e-4
allele num: 6488
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.317263381779511e-4
allele num: 11284
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.252252252252252e-3
allele num: 888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 159
allele frequency: 2.442396313364056e-3
allele num: 65100
num of homozygotes: 1

African
type: Population
allele count: 11
allele frequency: 1.083743842364532e-3
allele num: 10150
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.127450980392157e-5
allele num: 16320
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.13e0

MQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.1e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

DP
type: SiteQuality
SIO_000300: 1.883241e6

QD
type: SiteQuality
SIO_000300: 1.438e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.74e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e0

GenotypeQuality
all individuals: 325
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2056
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2115
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4682
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17888
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2638
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1884
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.221896383186706e-4
allele num: 8184
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.121076233183856e-3
allele num: 892
num of homozygotes: 0

African
type: Population
allele count: 271
allele frequency: 2.681044717055798e-2
allele num: 10108
num of homozygotes: 3

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16306
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6494
num of homozygotes: 0

Latino
type: Population
allele count: 17
allele frequency: 1.51326330781556e-3
allele num: 11234
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 2.0e-4
allele num: 65000
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.872564e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.524e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

QD
type: SiteQuality
SIO_000300: 1.456e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 6132
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1218
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 764
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1437
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1843
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13301
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8411
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 4342
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 7.5e0
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8148
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64806
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.336179295624333e-4
allele num: 11244
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16276
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10102
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6480
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.93e0

VQSLOD
type: SiteQuality
SIO_000300: 7.74e-1

FS
type: SiteQuality
SIO_000300: 6.117e0

QD
type: SiteQuality
SIO_000300: 1.467e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.65e-1

DP
type: SiteQuality
SIO_000300: 1.838769e6

GenotypeQuality
all individuals: 762
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5282
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10653
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1220
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1413
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8404
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4266
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 1.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64538
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8102
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.932459276916965e-5
allele num: 10068
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11194
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16240
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

DP
type: SiteQuality
SIO_000300: 1.830116e6

MQRankSum
type: SiteQuality
SIO_000300: 6.850000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.64e-1

MQ
type: SiteQuality
SIO_000300: 5.896e1

QD
type: SiteQuality
SIO_000300: 4.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.64e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.559e0

GenotypeQuality
all individuals: 391
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2771
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6454
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5653
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5676
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3595
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8405
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 384
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 760
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63800
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.508151492350138e-4
allele num: 7974
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9984
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11032
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16142
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.817901e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.97e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.014e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.036e1

GenotypeQuality
all individuals: 124
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2508
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1996
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2699
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4053
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.00792697573865e-5
allele num: 66608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.91e0

DP
type: SiteQuality
SIO_000300: 2.547454e6

MQRankSum
type: SiteQuality
SIO_000300: 4.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.53e-1

MQ
type: SiteQuality
SIO_000300: 6.031e1

FS
type: SiteQuality
SIO_000300: 6.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.0e-2

QD
type: SiteQuality
SIO_000300: 2.818e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3663
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2775
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2032
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3737
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4093
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16198001394376e-4
allele num: 8606
num of homozygotes: 0

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

European (Finnish)
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: 16508
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66622
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.55e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.43e-1

DP
type: SiteQuality
SIO_000300: 2.552762e6

VQSLOD
type: SiteQuality
SIO_000300: 1.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.237e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.03e0

MQRankSum
type: SiteQuality
SIO_000300: 1.35e0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 96
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GenotypeQuality
all individuals: 2055
bin: 7.25e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66664
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

DP
type: SiteQuality
SIO_000300: 2.558801e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

QD
type: SiteQuality
SIO_000300: 1.437e1

MQRankSum
type: SiteQuality
SIO_000300: -1.114e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.681e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.22e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500105007350515e-5
allele num: 66662
num of homozygotes: 0

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.639e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 2.559776e6

MQ
type: SiteQuality
SIO_000300: 5.948e1

QD
type: SiteQuality
SIO_000300: 9.69e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.399999999999999e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.94e-1

MQ
type: SiteQuality
SIO_000300: 5.929e1

VQSLOD
type: SiteQuality
SIO_000300: 8.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

FS
type: SiteQuality
SIO_000300: 5.582e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.94e-1

QD
type: SiteQuality
SIO_000300: 9.039999999999999e0

DP
type: SiteQuality
SIO_000300: 2.566975e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.661e0

GenotypeQuality
all individuals: 4205
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 25
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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: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 1.86e0

MQRankSum
type: SiteQuality
SIO_000300: 1.45e0

DP
type: SiteQuality
SIO_000300: 2.569511e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

QD
type: SiteQuality
SIO_000300: 2.14e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.52e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 75
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GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3412
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36908
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 32
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GenotypeQuality
all individuals: 4207
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.868e1

MQRankSum
type: SiteQuality
SIO_000300: 1.5e0

VQSLOD
type: SiteQuality
SIO_000300: -1.339e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.367e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.572239e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 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: 9.75e1
variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 3
allele frequency: 2.883506343713956e-4
allele num: 10404
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998410842253606e-5
allele num: 66702
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.41e-1

FS
type: SiteQuality
SIO_000300: 3.611e0

VQSLOD
type: SiteQuality
SIO_000300: 1.95e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.03e-1

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.84e0

DP
type: SiteQuality
SIO_000300: 2.572801e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 16
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.948e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.4e-2

FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.572355e6

VQSLOD
type: SiteQuality
SIO_000300: 4.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.6e-1

QD
type: SiteQuality
SIO_000300: 1.067e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3878
bin: 8.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

South Asian
type: Population
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allele frequency: 0.0e0
allele num: 16512
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African
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allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 6.34e-1

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.07e-1

DP
type: SiteQuality
SIO_000300: 2.572426e6

QD
type: SiteQuality
SIO_000300: 1.355e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.88e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 9.11e-1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.158e0

MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 7.4e-3

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 9.68e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.090000000000001e-1

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.013e1

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3886
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

African
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allele count: 3
allele frequency: 2.882952142994427e-4
allele num: 10406
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.956e1

QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.215e0

DP
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MQRankSum
type: SiteQuality
SIO_000300: 4.57e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.57e0

FS
type: SiteQuality
SIO_000300: 5.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.11e-1

GenotypeQuality
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variant carriers: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.953e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-1

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.129e0

VQSLOD
type: SiteQuality
SIO_000300: 1.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.679e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.5e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.44e-1

DP
type: SiteQuality
SIO_000300: 2.575637e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
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East Asian
type: Population
allele count: 1
allele frequency: 1.157675387821255e-4
allele num: 8638
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 4.68634e6

VQSLOD
type: SiteQuality
SIO_000300: 5.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.92e-1

QD
type: SiteQuality
SIO_000300: 2.021e1

MQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

MQ
type: SiteQuality
SIO_000300: 5.966e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.41e-2

FS
type: SiteQuality
SIO_000300: 5.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.28e-1

GenotypeQuality
all individuals: 700
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variant carriers: 11

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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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: 40205

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 2

South Asian
type: Population
allele count: 5086
allele frequency: 3.080184108527132e-1
allele num: 16512
num of homozygotes: 830

European (Non-Finnish)
type: Population
allele count: 32721
allele frequency: 4.904079613920446e-1
allele num: 66722
num of homozygotes: 8148

Other
type: Population
allele count: 374
allele frequency: 4.118942731277533e-1
allele num: 908
num of homozygotes: 74

African
type: Population
allele count: 6121
allele frequency: 5.882183355756294e-1
allele num: 10406
num of homozygotes: 1823

European (Finnish)
type: Population
allele count: 2553
allele frequency: 3.864668483197093e-1
allele num: 6606
num of homozygotes: 487

Latino
type: Population
allele count: 4300
allele frequency: 3.719079743988929e-1
allele num: 11562
num of homozygotes: 808

East Asian
type: Population
allele count: 1457
allele frequency: 1.686733040055568e-1
allele num: 8638
num of homozygotes: 129

VQSLOD
type: SiteQuality
SIO_000300: 5.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.28e-1

DP
type: SiteQuality
SIO_000300: 4.68634e6

QD
type: SiteQuality
SIO_000300: 2.021e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.22e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.41e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

FS
type: SiteQuality
SIO_000300: 5.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.92e-1

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495459585818323e-5
allele num: 66734
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.54e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.68e-1

QD
type: SiteQuality
SIO_000300: 1.657e1

FS
type: SiteQuality
SIO_000300: 1.129e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

DP
type: SiteQuality
SIO_000300: 3.990531e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.516e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.370000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.178e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.31e-1

GenotypeQuality
all individuals: 50995
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variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1907
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.49243264303054e-5
allele num: 66734
num of homozygotes: 1

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.958e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.370000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.68e-1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.990531e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.54e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.178e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.31e-1

FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.657e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.95e-1

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.95e1

FS
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SIO_000300: 1.907e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.061e0

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.990399e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
all individuals: 1909
bin: 9.25e1
variant carriers: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.24e-2

QD
type: SiteQuality
SIO_000300: 3.244e1

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

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

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

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

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

African
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allele count: 1
allele frequency: 9.611687812379854e-5
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66730
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South Asian
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InbreedingCoeff
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FS
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ClippingRankSum
type: SiteQuality
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VQSLOD
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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DP
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1909
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
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Other
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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FS
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ReadPosRankSum
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MQRankSum
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DP
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QD
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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South Asian
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Latino
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East Asian
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allele frequency: 0.0e0
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BaseQRankSum
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DP
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MQRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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FS
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InbreedingCoeff
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QD
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ClippingRankSum
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GenotypeQuality
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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African
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66740
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East Asian
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num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

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

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

African
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allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

South Asian
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QD
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MQRankSum
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MQ
type: SiteQuality
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VQSLOD
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

BaseQRankSum
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DP
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SIO_000300: 3.990713e6

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 6
allele frequency: 8.990110878034162e-5
allele num: 66740
num of homozygotes: 0

South Asian
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allele num: 16512
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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Other
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Latino
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FS
type: SiteQuality
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InbreedingCoeff
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DP
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.070000000000001e-1

MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 8.71e-1

VQSLOD
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GenotypeQuality
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variant carriers: 0

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

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

Latino
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allele frequency: 0.0e0
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East Asian
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European (Finnish)
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African
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allele frequency: 3.843936190659235e-4
allele num: 10406
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European (Non-Finnish)
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South Asian
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MQRankSum
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ClippingRankSum
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FS
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MQ
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DP
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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European (Finnish)
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European (Non-Finnish)
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South Asian
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African
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MQ
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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MQRankSum
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BaseQRankSum
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FS
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QD
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InbreedingCoeff
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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East Asian
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European (Finnish)
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Latino
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Other
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South Asian
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ReadPosRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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QD
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MQRankSum
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BaseQRankSum
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DP
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FS
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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African
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South Asian
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Latino
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European (Finnish)
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MQ
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ReadPosRankSum
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DP
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MQRankSum
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ClippingRankSum
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VQSLOD
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FS
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QD
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InbreedingCoeff
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BaseQRankSum
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Latino
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Other
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European (Non-Finnish)
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allele num: 66740
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European (Finnish)
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South Asian
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VQSLOD
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MQRankSum
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InbreedingCoeff
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QD
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FS
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ReadPosRankSum
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BaseQRankSum
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DP
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MQ
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SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.21e-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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
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European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495055439017081e-5
allele num: 66740
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.683e0

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.951e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.69e-1

DP
type: SiteQuality
SIO_000300: 3.99081e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.751e0

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: 3

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

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

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

South Asian
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allele count: 3
allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
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Other
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QD
type: SiteQuality
SIO_000300: 1.101e1

DP
type: SiteQuality
SIO_000300: 3.991232e6

FS
type: SiteQuality
SIO_000300: 1.168e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

VQSLOD
type: SiteQuality
SIO_000300: 9.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.97e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

Other
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MQRankSum
type: SiteQuality
SIO_000300: 7.69e-1

FS
type: SiteQuality
SIO_000300: 1.168e0

QD
type: SiteQuality
SIO_000300: 1.101e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.991232e6

MQ
type: SiteQuality
SIO_000300: 5.979e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 1.31e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-2

MQ
type: SiteQuality
SIO_000300: 5.934e1

QD
type: SiteQuality
SIO_000300: 1.127e1

FS
type: SiteQuality
SIO_000300: 1.266e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.41e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 3.990897e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
allele num: 908
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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ReadPosRankSum
type: SiteQuality
SIO_000300: -5.3e-2

MQ
type: SiteQuality
SIO_000300: 5.945e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.326e0

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.0465e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.67e-1

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 908
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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European (Non-Finnish)
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allele count: 3
allele frequency: 4.495055439017081e-5
allele num: 66740
num of homozygotes: 0

African
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allele frequency: 9.609840476648087e-5
allele num: 10406
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Latino
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num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e-2

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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