8-133984058-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984058
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984058
    reference: chr 8
allele count: 39125
allele frequency: 3.226165542490558e-1
allele num: 121274
alternate allele: T
annotation: Annotation
  canonical: false
  clinical significance: risk_factor
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.1105C>T
  hgvsp: ENSP00000441693.1:p.Arg369Trp
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: true
  clinical significance: risk_factor
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.5995C>T
  hgvsp: ENSP00000220616.4:p.Arg1999Trp
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  clinical significance: risk_factor
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.104C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  clinical significance: risk_factor
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.5824C>T
  hgvsp: ENSP00000367100.1:p.Arg1942Trp
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  clinical significance: risk_factor
  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.*2208C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  clinical significance: risk_factor
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.457C>T
  hgvsp: ENSP00000430430.1:p.Arg153Trp
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  clinical significance: risk_factor
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.132C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  clinical significance: risk_factor
  consequence: missense_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.1361C>T
  hgvsp: ENSP00000430523.1:p.Arg455Trp
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3311
  bin: 5.75e1
  variant carriers: 2836
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 8.75e1
  variant carriers: 1181
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 7.25e1
  variant carriers: 2268
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 9.25e1
  variant carriers: 991
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 4.25e1
  variant carriers: 1541
genotype depth: GenotypeDepth
  all individuals: 8698
  bin: 2.75e1
  variant carriers: 251
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 6.25e1
  variant carriers: 2847
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 3.75e1
  variant carriers: 959
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 7.75e1
  variant carriers: 1850
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4192
  bin: 3.25e1
  variant carriers: 572
genotype depth: GenotypeDepth
  all individuals: 9458
  bin: 9.75e1
  variant carriers: 8278
genotype depth: GenotypeDepth
  all individuals: 8824
  bin: 2.25e1
  variant carriers: 108
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 6.75e1
  variant carriers: 2516
genotype depth: GenotypeDepth
  all individuals: 2647
  bin: 4.75e1
  variant carriers: 2121
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 8.25e1
  variant carriers: 1470
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 5.25e1
  variant carriers: 2494
genotype quality: GenotypeQuality
  all individuals: 38120
  bin: 9.75e1
  variant carriers: 31868
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 8.75e1
  variant carriers: 47
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 9
hgvs: p.Arg1999Trp
num of homozygotes: 6808
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

8-133984059-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984059
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984059
    reference: chr 8
allele count: 4
allele frequency: 3.297011259293451e-5
allele num: 121322
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.5996G>A
  hgvsp: ENSP00000220616.4:p.Arg1999Gln
  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.5825G>A
  hgvsp: ENSP00000367100.1:p.Arg1942Gln
  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.1106G>A
  hgvsp: ENSP00000441693.1:p.Arg369Gln
  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.458G>A
  hgvsp: ENSP00000430430.1:p.Arg153Gln
  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.1362G>A
  hgvsp: ENSP00000430523.1:p.Arg455Gln
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.133G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.105G>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.*2209G>A
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20256
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3633
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11522
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2971
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10712
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1329
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7820
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27711
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg1999Gln
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

8-133984063-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984063
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984063
    reference: chr 8
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.6000C>T
  hgvsp: ENST00000220616.4:c.6000C>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.5829C>T
  hgvsp: ENST00000377869.1:c.5829C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.109C>T
  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.*2213C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.137C>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.1110C>T
  hgvsp: ENST00000542445.1:c.1110C>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.462C>T
  hgvsp: ENST00000519543.1:c.462C>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.1366C>T
  hgvsp: ENST00000519178.1:c.1366C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10709
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11523
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2969
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2219
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 918
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3421
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27739
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Cys2000Cys
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

8-133984064-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984064
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984064
    reference: chr 8
allele count: 32
allele frequency: 2.637435094370724e-4
allele num: 121330
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.5830G>A
  hgvsp: ENSP00000367100.1:p.Asp1944Asn
  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.1367G>A
  hgvsp: ENSP00000430523.1:p.Asp457Asn
  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.1111G>A
  hgvsp: ENSP00000441693.1:p.Asp371Asn
  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.6001G>A
  hgvsp: ENSP00000220616.4:p.Asp2001Asn
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.138G>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.463G>A
  hgvsp: ENSP00000430430.1:p.Asp155Asn
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.110G>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.*2214G>A
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20278
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3634
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11523
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3423
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7826
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp2001Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD

8-133984066-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984066
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984066
    reference: chr 8
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.112T>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.*2216T>C
  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.1369T>C
  hgvsp: ENST00000519178.1:c.1369T>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.6003T>C
  hgvsp: ENST00000220616.4:c.6003T>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.1113T>C
  hgvsp: ENST00000542445.1:c.1113T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.140T>C
  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.465T>C
  hgvsp: ENST00000519543.1:c.465T>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.5832T>C
  hgvsp: ENST00000377869.1:c.5832T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3633
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11529
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2967
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10704
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1325
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3424
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asp2001Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum

8-133984068-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984068
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984068
    reference: chr 8
allele count: 7
allele frequency: 5.769294168067781e-5
allele num: 121332
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.1115C>T
  hgvsp: ENSP00000441693.1:p.Ala372Val
  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.5834C>T
  hgvsp: ENSP00000367100.1:p.Ala1945Val
  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.1371C>T
  hgvsp: ENSP00000430523.1:p.Ala458Val
  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.6005C>T
  hgvsp: ENSP00000220616.4:p.Ala2002Val
  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.*2218C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.142C>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.467C>T
  hgvsp: ENSP00000430430.1:p.Ala156Val
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.114C>T
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11525
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10707
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 916
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27779
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1325
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala2002Val
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

8-133984081-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984081
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984081
    reference: chr 8
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
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.5847C>T
  hgvsp: ENST00000377869.1:c.5847C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.127C>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.1128C>T
  hgvsp: ENST00000542445.1:c.1128C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.155C>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.1384C>T
  hgvsp: ENST00000519178.1:c.1384C>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.6018C>T
  hgvsp: ENST00000220616.4:c.6018C>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.480C>T
  hgvsp: ENST00000519543.1:c.480C>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.*2231C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.10C>T
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10708
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20323
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11526
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3423
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 914
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27826
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Cys2006Cys
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

8-133984084-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984084
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984084
    reference: chr 8
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430430
  ensembl transcript: ENST00000519543
  gene symbol: TG
  hgvsc: ENST00000519543.1:c.483T>C
  hgvsp: ENST00000519543.1:c.483T>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.1131T>C
  hgvsp: ENST00000542445.1:c.1131T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.130T>C
  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.5850T>C
  hgvsp: ENST00000377869.1:c.5850T>C(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.1387T>C
  hgvsp: ENST00000519178.1:c.1387T>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.*2234T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.13T>C
  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.6021T>C
  hgvsp: ENST00000220616.4:c.6021T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.158T>C
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2967
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10705
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27818
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7830
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14387
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Thr2007Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD

8-133984091-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984091
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984091
    reference: chr 8
allele count: 1
allele frequency: 8.244702778464837e-6
allele num: 121290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.137G>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.1394G>A
  hgvsp: ENSP00000430523.1:p.Gly466Arg
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.20G>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.1138G>A
  hgvsp: ENSP00000441693.1:p.Gly380Arg
  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.490G>A
  hgvsp: ENSP00000430430.1:p.Gly164Arg
  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.6028G>A
  hgvsp: ENSP00000220616.4:p.Gly2010Arg
  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.5857G>A
  hgvsp: ENSP00000367100.1:p.Gly1953Arg
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.165G>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.*2241G>A
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11508
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10701
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3421
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7826
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly2010Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

8-133984107-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984107
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984107
    reference: chr 8
allele count: 1
allele frequency: 8.24905548314718e-6
allele num: 121226
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.506C>T
  hgvsp: ENSP00000430430.1:p.Ser169Phe
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.181C>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.1154C>T
  hgvsp: ENSP00000441693.1:p.Ser385Phe
  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.6044C>T
  hgvsp: ENSP00000220616.4:p.Ser2015Phe
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.36C>T
  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.*2257C>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.5873C>T
  hgvsp: ENSP00000367100.1:p.Ser1958Phe
  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.1410C>T
  hgvsp: ENSP00000430523.1:p.Ser471Phe
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.153C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.12C>T
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10681
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 912
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser2015Phe
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP

8-133984114-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984114
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984114
    reference: chr 8
allele count: 2
allele frequency: 1.650410126916539e-5
allele num: 121182
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.188A>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.*2264A>G
  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.6051A>G
  hgvsp: ENST00000220616.4:c.6051A>G(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.1161A>G
  hgvsp: ENST00000542445.1:c.1161A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.160A>G
  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.513A>G
  hgvsp: ENST00000519543.1:c.513A>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.5880A>G
  hgvsp: ENST00000377869.1:c.5880A>G(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.1417A>G
  hgvsp: ENST00000519178.1:c.1417A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.19A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.43A>G
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3621
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11413
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu2017Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

http://identifiers.org/exac.variant/8-133984116-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984116
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984116
    reference: chr 8
allele count: 1
allele frequency: 8.25218682950982e-6
allele num: 121180
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.190A>C
  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.515A>C
  hgvsp: ENSP00000430430.1:p.Lys172Thr
  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.*2266A>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.21A>C
  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.1163A>C
  hgvsp: ENSP00000441693.1:p.Lys388Thr
  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.5882A>C
  hgvsp: ENSP00000367100.1:p.Lys1961Thr
  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.1419A>C
  hgvsp: ENSP00000430523.1:p.Lys474Thr
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.45A>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.162A>C
  variant of: http://identifiers.org/hgnc/11764
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.6053A>C
  hgvsp: ENSP00000220616.4:p.Lys2018Thr
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10656
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3621
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20307
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys2018Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

8-133984122-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984122
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984122
    reference: chr 8
allele count: 1
allele frequency: 8.256547442121603e-6
allele num: 121116
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.47+4A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.192+4A>G
  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.517+4A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.23+4A>G
  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.*2268+4A>G
  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.1165+4A>G
  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.1421+4A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.164+4A>G
  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.6055+4A>G
  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.5884+4A>G
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10614
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3610
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20263
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: c.6055+4A>G
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

8-133984125-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984125
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984125
    reference: chr 8
allele count: 842
allele frequency: 6.954194816564529e-3
allele num: 121078
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.192+7A>G
  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.*2268+7A>G
  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.1421+7A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.47+7A>G
  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.517+7A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.23+7A>G
  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.1165+7A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.164+7A>G
  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.5884+7A>G
  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.6055+7A>G
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 8.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.75e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 5.25e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 20183
  bin: 2.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 7.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 6.75e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 4.75e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 7.25e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 6.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 3.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10583
  bin: 3.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 8.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11299
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2965
  bin: 9.75e1
  variant carriers: 192
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 9.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 4.25e1
  variant carriers: 64
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
hgvs: c.6055+7A>G
num of homozygotes: 28
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

8-133984135-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984135
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984135
    reference: chr 8
allele count: 13
allele frequency: 1.07566028993182e-4
allele num: 120856
alternate allele: T
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.*2268+17C>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.517+17C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.47+17C>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.6055+17C>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.1421+17C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.23+17C>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.1165+17C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.164+17C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.192+17C>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.5884+17C>T
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10483
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3604
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19902
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11095
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

8-133984144-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984144
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984144
    reference: chr 8
allele count: 1
allele frequency: 8.289811821271656e-6
allele num: 120630
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.23+26C>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.*2268+26C>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.1165+26C>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.517+26C>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.192+26C>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.5884+26C>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.1421+26C>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.164+26C>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.47+26C>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.6055+26C>G
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10640
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9903
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3517
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1234
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7272
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-133984149-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984149
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984149
    reference: chr 8
allele count: 8
allele frequency: 6.641429235571495e-5
allele num: 120456
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.1165+31C>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.*2268+31C>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.1421+31C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.47+31C>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.5884+31C>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.6055+31C>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.517+31C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.192+31C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.23+31C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.164+31C>T
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18274
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2889
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9408
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10066
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2463
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3189
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-133984150-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984150
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984150
    reference: chr 8
allele count: 41
allele frequency: 3.406617146085714e-4
allele num: 120354
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.1165+32G>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.517+32G>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.*2268+32G>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.5884+32G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.47+32G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.192+32G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.164+32G>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.1421+32G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.23+32G>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.6055+32G>A
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9888
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18062
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2691
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3424
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9308
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 22999
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

8-133984153-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984153
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984153
    reference: chr 8
allele count: 1
allele frequency: 8.315870006320061e-6
allele num: 120252
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.23+35C>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.1421+35C>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.1165+35C>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.6055+35C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.47+35C>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.*2268+35C>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.5884+35C>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.517+35C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.164+35C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.192+35C>T
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3244
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8158
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7291
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8434
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15460
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1957
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

8-133984794-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984794
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984794
    reference: chr 8
allele count: 1
allele frequency: 8.482339768601771e-6
allele num: 117892
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-49T>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.518-49T>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.*2269-49T>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.1166-49T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-49T>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.1422-49T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-49T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-49T>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.6056-49T>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.5885-49T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-49T>C
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7775
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6601
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9260
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3716
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5847
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8650
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1428
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

8-133984798-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984798
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984798
    reference: chr 8
allele count: 1
allele frequency: 8.492424757116652e-6
allele num: 117752
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-45C>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.1166-45C>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.5885-45C>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.*2269-45C>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.1422-45C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-45C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-45C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-45C>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.518-45C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-45C>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.6056-45C>T
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9530
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8694
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5905
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6773
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff

8-133984800-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984800
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984800
    reference: chr 8
allele count: 1
allele frequency: 8.488099684242691e-6
allele num: 117812
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-43G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-43G>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.5885-43G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-43G>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.1166-43G>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.6056-43G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-43G>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.1422-43G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-43G>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.*2269-43G>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.518-43G>A
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6769
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8795
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7886
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2048
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 776
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff

8-133984809-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984809
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984809
    reference: chr 8
allele count: 1
allele frequency: 8.487811502682149e-6
allele num: 117816
alternate allele: C
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.*2269-34T>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.6056-34T>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.5885-34T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-34T>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.518-34T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-34T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-34T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-34T>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.1166-34T>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.1422-34T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-34T>C
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8441
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6405
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9283
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5749
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

8-133984812-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984812
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984812
    reference: chr 8
allele count: 1
allele frequency: 8.675434639275428e-6
allele num: 115268
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-31T>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.*2269-31T>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.1166-31T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-31T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-31T>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.6056-31T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-31T>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.5885-31T>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.1422-31T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-31T>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.518-31T>C
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8341
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3331
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7175
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4936
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4516
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3120
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

8-133984813-G-GTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984813
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984816
    reference: chr 8
allele count: 1
allele frequency: 8.445232666159953e-6
allele num: 118410
alternate allele: GTTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.5885-30_5885-29insTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-30_117-29insTTT
  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.*2269-30_*2269-29insTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-30_193-29insTTT
  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.1166-30_1166-29insTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-30_24-29insTTT
  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.6056-30_6056-29insTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-30_165-29insTTT
  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.518-30_518-29insTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-30_48-29insTTT
  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.1422-30_1422-29insTTT
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6652
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10089
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10721
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum

8-133984813-GGTTTTTT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984813
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984806
    reference: chr 8
allele count: 60
allele frequency: 5.067139599695972e-4
allele num: 118410
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.1422-22_1422-16delGTTTTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-22_165-16delGTTTTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-22_117-16delGTTTTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-22_24-16delGTTTTTT
  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.*2269-22_*2269-16delGTTTTTT
  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.5885-22_5885-16delGTTTTTT
  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.6056-22_6056-16delGTTTTTT
  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.1166-22_1166-16delGTTTTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-22_48-16delGTTTTTT
  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.518-22_518-16delGTTTTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-22_193-16delGTTTTTT
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10089
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 1.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 2.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 7.5e0
  variant carriers: 100
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10721
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9041
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 2.5e0
  variant carriers: 149
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 1.25e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 6652
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5283
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4066
  bin: 7.75e1
  variant carriers: 3
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: GGTTTTTT
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

8-133984814-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984814
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984815
    reference: chr 8
allele count: 12137
allele frequency: 1.384996348365894e-1
allele num: 87632
alternate allele: GT
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.*2269-23dupT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-23dupT
  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.5885-23dupT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-23dupT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-23dupT
  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.1166-23dupT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-23dupT
  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.1422-23dupT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-23dupT
  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.518-23dupT
  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.6056-23dupT
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 8.25e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 7.25e1
  variant carriers: 180
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.5e0
  variant carriers: 334
genotype depth: GenotypeDepth
  all individuals: 6552
  bin: 3.75e1
  variant carriers: 1477
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.75e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 4853
  bin: 4.75e1
  variant carriers: 822
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 6.75e1
  variant carriers: 219
genotype depth: GenotypeDepth
  all individuals: 2869
  bin: 5.75e1
  variant carriers: 403
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 2.75e1
  variant carriers: 2449
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 1.25e1
  variant carriers: 874
genotype depth: GenotypeDepth
  all individuals: 4921
  bin: 2.25e1
  variant carriers: 2212
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 1.75e1
  variant carriers: 1615
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 6.25e1
  variant carriers: 327
genotype depth: GenotypeDepth
  all individuals: 5852
  bin: 4.25e1
  variant carriers: 1068
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 9.25e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 7.75e1
  variant carriers: 120
genotype depth: GenotypeDepth
  all individuals: 6958
  bin: 3.25e1
  variant carriers: 2130
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 5.25e1
  variant carriers: 552
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 9.75e1
  variant carriers: 129
genotype quality: GenotypeQuality
  all individuals: 1899
  bin: 1.75e1
  variant carriers: 777
num of homozygotes: 151
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP

8-133984814-G-GTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984814
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984816
    reference: chr 8
allele count: 5485
allele frequency: 6.259129085265656e-2
allele num: 87632
alternate allele: GTT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-24_48-23dupTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-24_117-23dupTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-24_193-23dupTT
  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.1422-24_1422-23dupTT
  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.5885-24_5885-23dupTT
  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.518-24_518-23dupTT
  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.1166-24_1166-23dupTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-24_165-23dupTT
  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.6056-24_6056-23dupTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-24_24-23dupTT
  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.*2269-24_*2269-23dupTT
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 4921
  bin: 2.25e1
  variant carriers: 1002
genotype depth: GenotypeDepth
  all individuals: 4853
  bin: 4.75e1
  variant carriers: 433
genotype depth: GenotypeDepth
  all individuals: 5852
  bin: 4.25e1
  variant carriers: 575
genotype depth: GenotypeDepth
  all individuals: 6552
  bin: 3.75e1
  variant carriers: 797
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 1.75e1
  variant carriers: 704
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 7.75e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.5e0
  variant carriers: 141
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 2.75e1
  variant carriers: 1086
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 7.25e1
  variant carriers: 133
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 5.25e1
  variant carriers: 317
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 1.25e1
  variant carriers: 389
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 6.75e1
  variant carriers: 156
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 6958
  bin: 3.25e1
  variant carriers: 998
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 9.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 2869
  bin: 5.75e1
  variant carriers: 251
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 8.25e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.75e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 6.25e1
  variant carriers: 172
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 9.75e1
  variant carriers: 127
genotype quality: GenotypeQuality
  all individuals: 1604
  bin: 4.25e1
  variant carriers: 329
num of homozygotes: 28
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

8-133984814-G-GTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984814
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984817
    reference: chr 8
allele count: 995
allele frequency: 1.135429979916012e-2
allele num: 87632
alternate allele: GTTT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-25_165-23dupTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-25_193-23dupTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-25_48-23dupTTT
  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.518-25_518-23dupTTT
  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.1422-25_1422-23dupTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-25_24-23dupTTT
  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.6056-25_6056-23dupTTT
  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.1166-25_1166-23dupTTT
  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.5885-25_5885-23dupTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-25_117-23dupTTT
  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.*2269-25_*2269-23dupTTT
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 7.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 7.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 6958
  bin: 3.25e1
  variant carriers: 173
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 8.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 5852
  bin: 4.25e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 1.25e1
  variant carriers: 111
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.5e0
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 1.75e1
  variant carriers: 166
genotype depth: GenotypeDepth
  all individuals: 4921
  bin: 2.25e1
  variant carriers: 182
genotype depth: GenotypeDepth
  all individuals: 6552
  bin: 3.75e1
  variant carriers: 154
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 6.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 9.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 6.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 4853
  bin: 4.75e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 9.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 2869
  bin: 5.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 5.25e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 2.75e1
  variant carriers: 210
genotype quality: GenotypeQuality
  all individuals: 1899
  bin: 1.75e1
  variant carriers: 99
num of homozygotes: 7
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD

8-133984814-G-GTTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984814
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984818
    reference: chr 8
allele count: 108
allele frequency: 1.232426510863611e-3
allele num: 87632
alternate allele: GTTTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.1422-26_1422-23dupTTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-26_48-23dupTTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-26_24-23dupTTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-26_193-23dupTTTT
  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.6056-26_6056-23dupTTTT
  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.*2269-26_*2269-23dupTTTT
  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.1166-26_1166-23dupTTTT
  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.518-26_518-23dupTTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-26_117-23dupTTTT
  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.5885-26_5885-23dupTTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-26_165-23dupTTTT
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4921
  bin: 2.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5852
  bin: 4.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 6958
  bin: 3.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 6552
  bin: 3.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 1.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2869
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 2.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 4853
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1847
  bin: 3.25e1
  variant carriers: 7
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

8-133984814-G-GTTTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984814
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984819
    reference: chr 8
allele count: 15
allele frequency: 1.711703487310571e-4
allele num: 87632
alternate allele: GTTTTT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-27_117-23dupTTTTT
  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.518-27_518-23dupTTTTT
  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.*2269-27_*2269-23dupTTTTT
  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.1166-27_1166-23dupTTTTT
  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.6056-27_6056-23dupTTTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-27_48-23dupTTTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-27_193-23dupTTTTT
  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.5885-27_5885-23dupTTTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-27_24-23dupTTTTT
  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.1422-27_1422-23dupTTTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-27_165-23dupTTTTT
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4853
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4921
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6958
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2869
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5852
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1430
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD

8-133984814-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984814
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984814
    reference: chr 8
allele count: 16
allele frequency: 1.825817053131276e-4
allele num: 87632
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.5885-29G>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-29G>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.1422-29G>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-29G>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.1166-29G>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-29G>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.518-29G>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-29G>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.6056-29G>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.*2269-29G>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-29G>T
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 2869
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4921
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4853
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6552
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6958
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5852
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1762
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

8-133984816-TTTTTG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984816
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984811
    reference: chr 8
allele count: 6
allele frequency: 1.384657989476599e-4
allele num: 43332
alternate allele: T
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.*2269-22_*2269-18delGTTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-22_165-18delGTTTT
  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.5885-22_5885-18delGTTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-22_24-18delGTTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-22_193-18delGTTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-22_48-18delGTTTT
  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.518-22_518-18delGTTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-22_117-18delGTTTT
  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.6056-22_6056-18delGTTTT
  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.1422-22_1422-18delGTTTT
  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.1166-22_1166-18delGTTTT
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 2657
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3620
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2844
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2571
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9960
  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
reference allele: TTTTTG
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

8-133984817-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984817
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984818
    reference: chr 8
allele count: 5
allele frequency: 8.609408361457401e-5
allele num: 58076
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-26_117-25insG
  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.518-26_518-25insG
  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.6056-26_6056-25insG
  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.1422-26_1422-25insG
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-26_165-25insG
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-26_48-25insG
  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.5885-26_5885-25insG
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-26_193-25insG
  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.1166-26_1166-25insG
  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.*2269-26_*2269-25insG
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-26_24-25insG
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3555
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2538
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2635
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3592
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1280
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

8-133984817-TTTTG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984817
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984813
    reference: chr 8
allele count: 86
allele frequency: 1.480818238170673e-3
allele num: 58076
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.518-22_518-19delGTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-22_165-19delGTTT
  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.5885-22_5885-19delGTTT
  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.1166-22_1166-19delGTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-22_48-19delGTTT
  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.*2269-22_*2269-19delGTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-22_193-19delGTTT
  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.1422-22_1422-19delGTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-22_117-19delGTTT
  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.6056-22_6056-19delGTTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-22_24-19delGTTT
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 3592
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 2.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 3.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3555
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2635
  bin: 3.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2538
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 7.5e0
  variant carriers: 18
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: TTTTG
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-133984818-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984818
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984818
    reference: chr 8
allele count: 4
allele frequency: 5.881315062047874e-5
allele num: 68012
alternate allele: G
canonical: false
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2989
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3702
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3775
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3033
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1572
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2215
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2307
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1499
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2379
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15498
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2399
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 508
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10182
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4016
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7990
  num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

8-133984818-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984818
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984819
    reference: chr 8
allele count: 1
allele frequency: 1.470328765511968e-5
allele num: 68012
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-25_117-24insG
  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.*2269-25_*2269-24insG
  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.5885-25_5885-24insG
  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.6056-25_6056-24insG
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-25_48-24insG
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-25_165-24insG
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-25_24-24insG
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-25_193-24insG
  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.1422-25_1422-24insG
  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.1166-25_1166-24insG
  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.518-25_518-24insG
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3775
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2989
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3033
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

8-133984818-TTTG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984818
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984815
    reference: chr 8
allele count: 479
allele frequency: 7.042874786802329e-3
allele num: 68012
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-22_24-20delGTT
  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.5885-22_5885-20delGTT
  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.6056-22_6056-20delGTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-22_165-20delGTT
  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.1422-22_1422-20delGTT
  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.518-22_518-20delGTT
  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.*2269-22_*2269-20delGTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-22_193-20delGTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-22_48-20delGTT
  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.1166-22_1166-20delGTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-22_117-20delGTT
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 2.25e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 3.25e1
  variant carriers: 139
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 2989
  bin: 3.75e1
  variant carriers: 130
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 4.25e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 5.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 2.75e1
  variant carriers: 126
genotype depth: GenotypeDepth
  all individuals: 3775
  bin: 4.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 3702
  bin: 5.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2307
  bin: 9.25e1
  variant carriers: 17
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: TTTG
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-133984819-TTG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984819
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984817
    reference: chr 8
allele count: 1737
allele frequency: 2.496981197170951e-2
allele num: 69564
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.1422-22_1422-21delGT
  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.*2269-22_*2269-21delGT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-22_117-21delGT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-22_165-21delGT
  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.5885-22_5885-21delGT
  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.518-22_518-21delGT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-22_193-21delGT
  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.1166-22_1166-21delGT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-22_48-21delGT
  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.6056-22_6056-21delGT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-22_24-21delGT
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 7.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 4.75e1
  variant carriers: 222
genotype depth: GenotypeDepth
  all individuals: 3533
  bin: 5.25e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 2.75e1
  variant carriers: 440
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 5.75e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 3.25e1
  variant carriers: 509
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 6.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 2.25e1
  variant carriers: 327
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 1.75e1
  variant carriers: 186
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4270
  bin: 4.25e1
  variant carriers: 273
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.5e0
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 4043
  bin: 3.75e1
  variant carriers: 372
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 8.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 6.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 2315
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 2080
  bin: 6.75e1
  variant carriers: 69
num of homozygotes: 3
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: TTG
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

8-133984820-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984820
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984819
    reference: chr 8
allele count: 5223
allele frequency: 7.581431806305522e-2
allele num: 68892
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430523
  ensembl transcript: ENST00000519178
  gene symbol: TG
  hgvsc: ENST00000519178.1:c.1422-22delG
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-22delG
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-22delG
  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.*2269-22delG
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-22delG
  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.6056-22delG
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-22delG
  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.1166-22delG
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-22delG
  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.518-22delG
  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.5885-22delG
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 4255
  bin: 2.75e1
  variant carriers: 1270
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 4.25e1
  variant carriers: 730
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 2.25e1
  variant carriers: 970
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 9.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 9.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 7.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 8.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 5.25e1
  variant carriers: 283
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 1.25e1
  variant carriers: 334
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 5.75e1
  variant carriers: 194
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 8.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 1.75e1
  variant carriers: 610
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 6.75e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 101
genotype depth: GenotypeDepth
  all individuals: 5156
  bin: 3.75e1
  variant carriers: 933
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 4.75e1
  variant carriers: 461
genotype depth: GenotypeDepth
  all individuals: 5254
  bin: 3.25e1
  variant carriers: 1262
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 6.25e1
  variant carriers: 118
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 7.25e1
  variant carriers: 42
genotype quality: GenotypeQuality
  all individuals: 1270
  bin: 2.75e1
  variant carriers: 483
num of homozygotes: 47
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: TG
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-133984821-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984821
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984821
    reference: chr 8
allele count: 41027
allele frequency: 3.951819530331927e-1
allele num: 103818
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.1166-22G>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-22G>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.1422-22G>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.*2269-22G>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-22G>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-22G>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-22G>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-22G>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.6056-22G>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.518-22G>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.5885-22G>T
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 7.25e1
  variant carriers: 967
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 8.75e1
  variant carriers: 497
genotype depth: GenotypeDepth
  all individuals: 5419
  bin: 4.75e1
  variant carriers: 3643
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 6.75e1
  variant carriers: 1259
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.5e0
  variant carriers: 474
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 1.25e1
  variant carriers: 1084
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 2.75e1
  variant carriers: 4221
genotype depth: GenotypeDepth
  all individuals: 4611
  bin: 5.25e1
  variant carriers: 2828
genotype depth: GenotypeDepth
  all individuals: 5787
  bin: 4.25e1
  variant carriers: 4181
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 7.75e1
  variant carriers: 759
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 121
genotype depth: GenotypeDepth
  all individuals: 3716
  bin: 2.25e1
  variant carriers: 3149
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 5.75e1
  variant carriers: 2158
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 9.25e1
  variant carriers: 406
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 9.75e1
  variant carriers: 1159
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 1.75e1
  variant carriers: 1936
genotype depth: GenotypeDepth
  all individuals: 5808
  bin: 3.25e1
  variant carriers: 4676
genotype depth: GenotypeDepth
  all individuals: 6129
  bin: 3.75e1
  variant carriers: 4735
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 8.25e1
  variant carriers: 614
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 6.25e1
  variant carriers: 1611
genotype quality: GenotypeQuality
  all individuals: 1771
  bin: 1.25e1
  variant carriers: 562
num of homozygotes: 2869
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

8-133984821-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984821
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984822
    reference: chr 8
allele count: 3115
allele frequency: 3.000443083087711e-2
allele num: 103818
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-10dupT
  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.6056-10dupT
  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.1166-10dupT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-10dupT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-10dupT
  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.1422-10dupT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-10dupT
  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.5885-10dupT
  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.518-10dupT
  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.*2269-10dupT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-10dupT
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 2.75e1
  variant carriers: 161
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3716
  bin: 2.25e1
  variant carriers: 114
genotype depth: GenotypeDepth
  all individuals: 5787
  bin: 4.25e1
  variant carriers: 314
genotype depth: GenotypeDepth
  all individuals: 5808
  bin: 3.25e1
  variant carriers: 200
genotype depth: GenotypeDepth
  all individuals: 6129
  bin: 3.75e1
  variant carriers: 274
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 1.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 9.75e1
  variant carriers: 674
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 6.75e1
  variant carriers: 256
genotype depth: GenotypeDepth
  all individuals: 4611
  bin: 5.25e1
  variant carriers: 362
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 7.75e1
  variant carriers: 166
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 5.75e1
  variant carriers: 330
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 1.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 8.75e1
  variant carriers: 121
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 9.25e1
  variant carriers: 110
genotype depth: GenotypeDepth
  all individuals: 5419
  bin: 4.75e1
  variant carriers: 333
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 6.25e1
  variant carriers: 331
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 7.25e1
  variant carriers: 199
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 8.25e1
  variant carriers: 127
genotype quality: GenotypeQuality
  all individuals: 1080
  bin: 7.75e1
  variant carriers: 114
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum

8-133984821-G-GTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984821
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984823
    reference: chr 8
allele count: 12
allele frequency: 1.155868924463966e-4
allele num: 103818
alternate allele: GTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000367100
  ensembl transcript: ENST00000377869
  gene symbol: TG
  hgvsc: ENST00000377869.1:c.5885-11_5885-10dupTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-11_165-10dupTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-11_117-10dupTT
  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.1422-11_1422-10dupTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-11_48-10dupTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-11_193-10dupTT
  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.6056-11_6056-10dupTT
  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.1166-11_1166-10dupTT
  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.*2269-11_*2269-10dupTT
  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.518-11_518-10dupTT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-11_24-10dupTT
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5787
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5419
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6129
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4611
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3716
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5808
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1205
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

8-133984821-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984821
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984820
    reference: chr 8
allele count: 6813
allele frequency: 6.562445818644166e-2
allele num: 103818
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.6056-10delT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-10delT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-10delT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-10delT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-10delT
  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.*2269-10delT
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-10delT
  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.1422-10delT
  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.518-10delT
  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.5885-10delT
  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.1166-10delT
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 8.75e1
  variant carriers: 259
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6129
  bin: 3.75e1
  variant carriers: 460
genotype depth: GenotypeDepth
  all individuals: 5419
  bin: 4.75e1
  variant carriers: 705
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 9.25e1
  variant carriers: 187
genotype depth: GenotypeDepth
  all individuals: 5787
  bin: 4.25e1
  variant carriers: 588
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 1.75e1
  variant carriers: 142
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 2.75e1
  variant carriers: 283
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 5.75e1
  variant carriers: 836
genotype depth: GenotypeDepth
  all individuals: 3716
  bin: 2.25e1
  variant carriers: 192
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 8.25e1
  variant carriers: 315
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 7.75e1
  variant carriers: 433
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 6.75e1
  variant carriers: 727
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 1.25e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 4611
  bin: 5.25e1
  variant carriers: 772
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 6.25e1
  variant carriers: 757
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 7.25e1
  variant carriers: 543
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 9.75e1
  variant carriers: 735
genotype depth: GenotypeDepth
  all individuals: 5808
  bin: 3.25e1
  variant carriers: 366
genotype quality: GenotypeQuality
  all individuals: 1493
  bin: 3.75e1
  variant carriers: 360
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: GT
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

8-133984821-GTT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984821
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984819
    reference: chr 8
allele count: 64
allele frequency: 6.164634263807817e-4
allele num: 103818
alternate allele: G
canonical: false
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 4611
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5787
  bin: 4.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 5808
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 3716
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6129
  bin: 3.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5419
  bin: 4.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1597
  bin: 3.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 2500
  bin: 2.5e0
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 1301
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1493
  bin: 3.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 1704
  bin: 1.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 1387
  bin: 4.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 1257
  bin: 6.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1771
  bin: 1.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 904
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1205
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1817
  bin: 7.5e0
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 1722
  bin: 2.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 983
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1059
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1638
  bin: 2.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1400
  bin: 4.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 940
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32988
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1080
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1251
  bin: 5.25e1
  variant carriers: 4
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 802
  num of homozygotes: 0
population: African
  type: Population
  allele count: 4
  allele frequency: 4.600874166091557e-4
  allele num: 8694
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 25
  allele frequency: 4.30366672404889e-4
  allele num: 58090
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 2
  allele frequency: 3.434065934065934e-4
  allele num: 5824
  num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
reference allele: GTT
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-133984822-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984822
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984822
    reference: chr 8
allele count: 2
allele frequency: 3.03030303030303e-4
allele num: 6600
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-21T>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.1166-21T>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-21T>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.1422-21T>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.6056-21T>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.5885-21T>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.*2269-21T>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-21T>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.518-21T>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-21T>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-21T>G
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: FS

8-133984826-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984826
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984826
    reference: chr 8
allele count: 1
allele frequency: 8.284043275842073e-6
allele num: 120714
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-17T>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-17T>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-17T>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.1422-17T>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-17T>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-17T>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.5885-17T>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.518-17T>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.1166-17T>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.*2269-17T>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.6056-17T>A
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4465
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6277
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3002
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4756
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4033
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5955
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

8-133984833-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984833
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984833
    reference: chr 8
allele count: 7
allele frequency: 5.783212161269002e-5
allele num: 121040
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-10T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-10T>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.6056-10T>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.*2269-10T>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.1422-10T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-10T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-10T>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.5885-10T>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.1166-10T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-10T>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.518-10T>C
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6408
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4750
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5969
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4035
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3643
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4756
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6359
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

8-133984834-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984834
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984834
    reference: chr 8
allele count: 16
allele frequency: 1.495858342214992e-4
allele num: 106962
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.1166-9C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-9C>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.518-9C>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.1422-9C>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.5885-9C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-9C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-9C>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.*2269-9C>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.6056-9C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-9C>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-9C>T
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6051
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4151
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5218
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2652
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5386
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6020
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6331
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4366
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5218
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5914
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/8-133984834-CCA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984834
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984832
    reference: chr 8
allele count: 2
allele frequency: 1.86982292776874e-5
allele num: 106962
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-7_48-6delAC
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-7_165-6delAC
  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.6056-7_6056-6delAC
  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.1422-7_1422-6delAC
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-7_193-6delAC
  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.1166-7_1166-6delAC
  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.518-7_518-6delAC
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-7_117-6delAC
  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.5885-7_5885-6delAC
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-7_24-6delAC
  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.*2269-7_*2269-6delAC
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5386
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2652
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6331
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4151
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6020
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5218
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6051
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.6056-7_6056-6delAC
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: CCA
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/8-133984836-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984836
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984836
    reference: chr 8
allele count: 6238
allele frequency: 5.750686800523628e-2
allele num: 108474
alternate allele: C
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.518-7A>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-7A>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-7A>C
  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.1166-7A>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-7A>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.1422-7A>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-7A>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.*2269-7A>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.5885-7A>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.6056-7A>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-7A>C
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 2.25e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 5591
  bin: 5.75e1
  variant carriers: 605
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 2420
  bin: 8.75e1
  variant carriers: 499
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 7.25e1
  variant carriers: 707
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 3.75e1
  variant carriers: 129
genotype depth: GenotypeDepth
  all individuals: 7514
  bin: 9.75e1
  variant carriers: 1567
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 3.25e1
  variant carriers: 124
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 2.75e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 4.75e1
  variant carriers: 334
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5458
  bin: 5.25e1
  variant carriers: 430
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 4.25e1
  variant carriers: 232
genotype depth: GenotypeDepth
  all individuals: 4855
  bin: 6.75e1
  variant carriers: 720
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 9.25e1
  variant carriers: 428
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 8.25e1
  variant carriers: 533
genotype quality: GenotypeQuality
hgvs: c.6056-7A>C
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

http://identifiers.org/exac.variant/8-133984838-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984838
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984838
    reference: chr 8
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: A
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.*2269-5C>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-5C>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-5C>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.6056-5C>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.518-5C>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.1166-5C>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-5C>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.1422-5C>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-5C>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.5885-5C>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-5C>A
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4712
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5624
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5795
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2948
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3851
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.6056-5C>A
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: C
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

8-133984840-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984840
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984840
    reference: chr 8
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165-3C>G
  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.518-3C>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48-3C>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24-3C>G
  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.*2269-3C>G
  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.5885-3C>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117-3C>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193-3C>G
  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.1422-3C>G
  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.1166-3C>G
  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.6056-3C>G
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3851
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5795
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2969
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4710
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5150
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2947
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.6056-3C>G
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

8-133984843-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984843
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984843
    reference: chr 8
allele count: 1
allele frequency: 8.239811473113496e-6
allele num: 121362
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.117G>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.193G>C
  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.518G>C
  hgvsp: ENSP00000430430.1:p.Gly173Ala
  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.1166G>C
  hgvsp: ENSP00000441693.1:p.Gly389Ala
  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.1422G>C
  hgvsp: ENSP00000430523.1:p.Gly475Ala
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.165G>C
  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.5885G>C
  hgvsp: ENSP00000367100.1:p.Gly1962Ala
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.48G>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.24G>C
  variant of: http://identifiers.org/hgnc/11764
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.6056G>C
  hgvsp: ENSP00000220616.4:p.Gly2019Ala
  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.*2269G>C
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3632
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4710
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4938
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6449
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5607
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly2019Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

8-133984844-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984844
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984844
    reference: chr 8
allele count: 22
allele frequency: 1.818392210669003e-4
allele num: 120986
alternate allele: G
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.1423A>G
  hgvsp: ENST00000519178.1:c.1423A>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.5886A>G
  hgvsp: ENST00000377869.1:c.5886A>G(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.*2270A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.49A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.25A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.118A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.166A>G
  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.6057A>G
  hgvsp: ENST00000220616.4:c.6057A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.194A>G
  variant of: http://identifiers.org/hgnc/11764
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.519A>G
  hgvsp: ENST00000519543.1:c.519A>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: ENSP00000441693
  ensembl transcript: ENST00000542445
  gene symbol: TG
  hgvsc: ENST00000542445.1:c.1167A>G
  hgvsp: ENST00000542445.1:c.1167A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2971
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6452
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3634
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4938
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5793
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4702
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.6057A>G
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

8-133984845-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984845
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984845
    reference: chr 8
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
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.6058G>A
  hgvsp: ENSP00000220616.4:p.Gly2020Arg
  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.1168G>A
  hgvsp: ENSP00000441693.1:p.Gly390Arg
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.26G>A
  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.520G>A
  hgvsp: ENSP00000430430.1:p.Gly174Arg
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.50G>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.1424G>A
  hgvsp: ENSP00000430523.1:p.Gly476Arg
  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.5887G>A
  hgvsp: ENSP00000367100.1:p.Gly1963Arg
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.119G>A
  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.*2271G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.167G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.195G>A
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6449
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5589
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5794
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5184
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6187
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4695
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly2020Arg
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

8-133984847-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984847
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984847
    reference: chr 8
allele count: 10
allele frequency: 8.249327679794097e-5
allele num: 121222
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.121A>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.*2273A>G
  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.6060A>G
  hgvsp: ENST00000220616.4:c.6060A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.52A>G
  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.5889A>G
  hgvsp: ENST00000377869.1:c.5889A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.197A>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.1170A>G
  hgvsp: ENST00000542445.1:c.1170A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.28A>G
  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.522A>G
  hgvsp: ENST00000519543.1:c.522A>G(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.1426A>G
  hgvsp: ENST00000519178.1:c.1426A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.169A>G
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3867
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5797
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4700
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6453
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5582
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5157
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Gly2020Gly
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

8-133984849-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984849
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984849
    reference: chr 8
allele count: 9
allele frequency: 7.430033847931974e-5
allele num: 121130
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.199A>G
  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.524A>G
  hgvsp: ENSP00000430430.1:p.Glu175Gly
  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.6062A>G
  hgvsp: ENSP00000220616.4:p.Glu2021Gly
  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.1172A>G
  hgvsp: ENSP00000441693.1:p.Glu391Gly
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.123A>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.1428A>G
  hgvsp: ENSP00000430523.1:p.Glu477Gly
  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.*2275A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.54A>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.5891A>G
  hgvsp: ENSP00000367100.1:p.Glu1964Gly
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.171A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.30A>G
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6449
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5798
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2989
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5165
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4699
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5583
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu2021Gly
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD

8-133984852-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984852
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984852
    reference: chr 8
allele count: 10
allele frequency: 8.27417299640901e-5
allele num: 120858
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.126T>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.5894T>G
  hgvsp: ENSP00000367100.1:p.Val1965Gly
  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.*2278T>G
  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.527T>G
  hgvsp: ENSP00000430430.1:p.Val176Gly
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.33T>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.57T>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.174T>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.1431T>G
  hgvsp: ENSP00000430523.1:p.Val478Gly
  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.6065T>G
  hgvsp: ENSP00000220616.4:p.Val2022Gly
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.202T>G
  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.1175T>G
  hgvsp: ENSP00000441693.1:p.Val392Gly
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4682
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5578
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4922
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5195
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5795
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6440
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6184
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val2022Gly
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

8-133984856-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984856
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984856
    reference: chr 8
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: G
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.*2282A>G
  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.531A>G
  hgvsp: ENST00000519543.1:c.531A>G(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.1179A>G
  hgvsp: ENST00000542445.1:c.1179A>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.6069A>G
  hgvsp: ENST00000220616.4:c.6069A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.130A>G
  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.5898A>G
  hgvsp: ENST00000377869.1:c.5898A>G(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.1435A>G
  hgvsp: ENST00000519178.1:c.1435A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.37A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.178A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.61A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.206A>G
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2124
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4699
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6485
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4982
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr2023Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

8-133984858-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984858
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984858
    reference: chr 8
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.180G>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.132G>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.1181G>T
  hgvsp: ENSP00000441693.1:p.Cys394Phe
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.208G>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.63G>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.5900G>T
  hgvsp: ENSP00000367100.1:p.Cys1967Phe
  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.*2284G>T
  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.6071G>T
  hgvsp: ENSP00000220616.4:p.Cys2024Phe
  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.1437G>T
  hgvsp: ENSP00000430523.1:p.Cys480Phe
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.39G>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.533G>T
  hgvsp: ENSP00000430430.1:p.Cys178Phe
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4984
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4699
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5050
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys2024Phe
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/8-133984863-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984863
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984863
    reference: chr 8
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.137A>C
  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.5905A>C
  hgvsp: ENSP00000367100.1:p.Thr1969Pro
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.44A>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.6076A>C
  hgvsp: ENSP00000220616.4:p.Thr2026Pro
  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.1442A>C
  hgvsp: ENSP00000430523.1:p.Thr482Pro
  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.*2289A>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.68A>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.213A>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.185A>C
  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.538A>C
  hgvsp: ENSP00000430430.1:p.Thr180Pro
  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.1186A>C
  hgvsp: ENSP00000441693.1:p.Thr396Pro
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5050
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4699
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4985
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6198
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr2026Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

8-133984865-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984865
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984865
    reference: chr 8
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.215T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.46T>C
  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.1188T>C
  hgvsp: ENST00000542445.1:c.1188T>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.5907T>C
  hgvsp: ENST00000377869.1:c.5907T>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.*2291T>C
  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.540T>C
  hgvsp: ENST00000519543.1:c.540T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.187T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.139T>C
  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.6078T>C
  hgvsp: ENST00000220616.4:c.6078T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.70T>C
  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.1444T>C
  hgvsp: ENST00000519178.1:c.1444T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4699
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6488
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6198
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr2026Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum

8-133984872-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984872
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984872
    reference: chr 8
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.146A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.53A>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.1451A>G
  hgvsp: ENSP00000430523.1:p.Ser485Gly
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.77A>G
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.194A>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.*2298A>G
  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.547A>G
  hgvsp: ENSP00000430430.1:p.Ser183Gly
  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.5914A>G
  hgvsp: ENSP00000367100.1:p.Ser1972Gly
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.222A>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.6085A>G
  hgvsp: ENSP00000220616.4:p.Ser2029Gly
  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.1195A>G
  hgvsp: ENSP00000441693.1:p.Ser399Gly
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4699
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4985
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5842
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser2029Gly
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

8-133984877-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984877
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984877
    reference: chr 8
allele count: 11
allele frequency: 9.06065698000066e-5
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430087
  ensembl transcript: ENST00000522797
  gene symbol: TG
  hgvsc: ENST00000522797.1:c.1G>A
  hgvsp: ENST00000522797.1:c.1G>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.6090G>A
  hgvsp: ENST00000220616.4:c.6090G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.199G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.227G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.82G>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.1200G>A
  hgvsp: ENST00000542445.1:c.1200G>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.552G>A
  hgvsp: ENST00000519543.1:c.552G>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.*2303G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.58G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.151G>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.5919G>A
  hgvsp: ENST00000377869.1:c.5919G>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.1456G>A
  hgvsp: ENST00000519178.1:c.1456G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5599
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5057
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4699
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu2030Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

8-133984889-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984889
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984889
    reference: chr 8
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
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.1212G>T
  hgvsp: ENSP00000441693.1:p.Met404Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.211G>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.1468G>T
  hgvsp: ENSP00000430523.1:p.Met490Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.94G>T
  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.6102G>T
  hgvsp: ENSP00000220616.4:p.Met2034Ile
  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.5931G>T
  hgvsp: ENSP00000367100.1:p.Met1977Ile
  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.564G>T
  hgvsp: ENSP00000430430.1:p.Met188Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.239G>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.70G>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430087
  ensembl transcript: ENST00000522797
  gene symbol: TG
  hgvsc: ENST00000522797.1:c.13G>T
  hgvsp: ENSP00000430087.1:p.Met5Ile
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.163G>T
  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.*2315G>T
  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: 2907
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5599
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4700
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6490
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met2034Ile
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

8-133984893-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984893
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984893
    reference: chr 8
allele count: 3
allele frequency: 2.471047559428694e-5
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.98A>T
  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.6106A>T
  hgvsp: ENSP00000220616.4:p.Ser2036Cys
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430087
  ensembl transcript: ENST00000522797
  gene symbol: TG
  hgvsc: ENST00000522797.1:c.17A>T
  hgvsp: ENSP00000430087.1:p.Ser7Cys
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.243A>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.74A>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.1472A>T
  hgvsp: ENSP00000430523.1:p.Ser492Cys
  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.5935A>T
  hgvsp: ENSP00000367100.1:p.Ser1979Cys
  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.1216A>T
  hgvsp: ENSP00000441693.1:p.Ser406Cys
  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.568A>T
  hgvsp: ENSP00000430430.1:p.Ser190Cys
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.167A>T
  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.*2319A>T
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.215A>T
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4700
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3056
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5599
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5051
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6491
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser2036Cys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

8-133984904-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984904
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984904
    reference: chr 8
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000220616
  ensembl transcript: ENST00000220616
  gene symbol: TG
  hgvsc: ENST00000220616.4:c.6117T>C
  hgvsp: ENST00000220616.4:c.6117T>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.1227T>C
  hgvsp: ENST00000542445.1:c.1227T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.85T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430087
  ensembl transcript: ENST00000522797
  gene symbol: TG
  hgvsc: ENST00000522797.1:c.28T>C
  hgvsp: ENST00000522797.1:c.28T>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.579T>C
  hgvsp: ENST00000519543.1:c.579T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.109T>C
  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.5946T>C
  hgvsp: ENST00000377869.1:c.5946T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.226T>C
  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.1483T>C
  hgvsp: ENST00000519178.1:c.1483T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.178T>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.*2330T>C
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.254T>C
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 8.25e1
  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: 6491
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5845
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn2039Asn
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

8-133984908-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 133984908
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 133984908
    reference: chr 8
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000519294
  gene symbol: TG
  hgvsc: ENST00000519294.1:n.113G>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.583G>A
  hgvsp: ENSP00000430430.1:p.Gly195Arg
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520197
  gene symbol: TG
  hgvsc: ENST00000520197.1:n.258G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000042832
  ensembl protein: ENSP00000430087
  ensembl transcript: ENST00000522797
  gene symbol: TG
  hgvsc: ENST00000522797.1:c.32G>A
  hgvsp: ENSP00000430087.1:p.Gly12Arg
  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.1487G>A
  hgvsp: ENSP00000430523.1:p.Gly497Arg
  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.5950G>A
  hgvsp: ENSP00000367100.1:p.Gly1984Arg
  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.1231G>A
  hgvsp: ENSP00000441693.1:p.Gly411Arg
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000522523
  gene symbol: TG
  hgvsc: ENST00000522523.1:n.182G>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.*2334G>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.6121G>A
  hgvsp: ENSP00000220616.4:p.Gly2041Arg
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000520089
  gene symbol: TG
  hgvsc: ENST00000520089.1:n.230G>A
  variant of: http://identifiers.org/hgnc/11764
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000042832
  ensembl transcript: ENST00000524151
  gene symbol: TG
  hgvsc: ENST00000524151.1:n.89G>A
  variant of: http://identifiers.org/hgnc/11764
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5845
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly2041Arg
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 1554
bin: 7.75e1
variant carriers: 48

GenotypeQuality
all individuals: 988
bin: 8.25e1
variant carriers: 64

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 11

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 9

GenotypeQuality
all individuals: 649
bin: 9.25e1
variant carriers: 81

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 8

GenotypeQuality
all individuals: 50
bin: 2.25e1
variant carriers: 9

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 6

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 7

GenotypeQuality
all individuals: 49
bin: 5.25e1
variant carriers: 30

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 22

GenotypeQuality
all individuals: 14020
bin: 6.25e1
variant carriers: 28

GenotypeQuality
all individuals: 1196
bin: 7.25e1
variant carriers: 39

GenotypeQuality
all individuals: 3460
bin: 6.75e1
variant carriers: 31

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 8

European (Non-Finnish)
type: Population
allele count: 23207
allele frequency: 3.480980380392392e-1
allele num: 66668
num of homozygotes: 4063

South Asian
type: Population
allele count: 4531
allele frequency: 2.7447298279622e-1
allele num: 16508
num of homozygotes: 629

Latino
type: Population
allele count: 2201
allele frequency: 1.904308703928015e-1
allele num: 11558
num of homozygotes: 228

African
type: Population
allele count: 5279
allele frequency: 5.074985579696212e-1
allele num: 10402
num of homozygotes: 1350

Other
type: Population
allele count: 314
allele frequency: 3.458149779735683e-1
allele num: 908
num of homozygotes: 56

European (Finnish)
type: Population
allele count: 2122
allele frequency: 3.209316394434362e-1
allele num: 6612
num of homozygotes: 340

East Asian
type: Population
allele count: 1471
allele frequency: 1.706892550475748e-1
allele num: 8618
num of homozygotes: 142

DP
type: SiteQuality
SIO_000300: 3.767229e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.97e-1

FS
type: SiteQuality
SIO_000300: 5.38e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.36e-2

MQ
type: SiteQuality
SIO_000300: 5.959e1

VQSLOD
type: SiteQuality
SIO_000300: 4.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.644e1

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2665
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3423
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2223
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14455
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 921
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.090000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.03e-1

QD
type: SiteQuality
SIO_000300: 2.246e1

MQ
type: SiteQuality
SIO_000300: 5.94e1

FS
type: SiteQuality
SIO_000300: 5.26e-1

DP
type: SiteQuality
SIO_000300: 2.352152e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.597e-1

GenotypeQuality
all individuals: 2664
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7823
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1327
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14446
bin: 9.75e1
variant carriers: 1

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: 8618
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
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: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.289e1

MQRankSum
type: SiteQuality
SIO_000300: -3.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.63e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.389e0

FS
type: SiteQuality
SIO_000300: 7.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

DP
type: SiteQuality
SIO_000300: 2.351831e6

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

GenotypeQuality
all individuals: 1326
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14447
bin: 9.75e1
variant carriers: 32

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

GenotypeQuality
all individuals: 2220
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 917
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27758
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2662
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 27
allele frequency: 4.047369210013491e-4
allele num: 66710
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.593809441466367e-4
allele num: 11566
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.64e-1

DP
type: SiteQuality
SIO_000300: 2.351878e6

FS
type: SiteQuality
SIO_000300: 1.124e0

MQRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

MQ
type: SiteQuality
SIO_000300: 5.957e1

QD
type: SiteQuality
SIO_000300: 1.582e1

GenotypeQuality
all individuals: 46
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 918
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2219
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2665
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27775
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14417
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7831
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 2.35029e6

VQSLOD
type: SiteQuality
SIO_000300: -2.37e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.707e0

QD
type: SiteQuality
SIO_000300: 1.71e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e0

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-2

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

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2659
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7829
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2216
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3422
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14416
bin: 9.75e1
variant carriers: 7

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
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: 11568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.497211728728189e-5
allele num: 66708
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.319647413593134e-4
allele num: 8622
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.350592e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.43e0

FS
type: SiteQuality
SIO_000300: 5.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.66e-1

QD
type: SiteQuality
SIO_000300: 1.282e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.66e0

MQ
type: SiteQuality
SIO_000300: 5.957e1

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

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

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2651
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.277e0

QD
type: SiteQuality
SIO_000300: 2.445e1

DP
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e0

MQRankSum
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SIO_000300: 1.36e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16504
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: 6608
num of homozygotes: 0

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

Latino
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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
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.69e-1

VQSLOD
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ClippingRankSum
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FS
type: SiteQuality
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MQRankSum
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.9e-1

InbreedingCoeff
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.932e1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499385252046661e-5
allele num: 66694
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16502
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African
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allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.086e1

FS
type: SiteQuality
SIO_000300: 9.29e-1

ReadPosRankSum
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SIO_000300: 1.11e-1

MQ
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SIO_000300: 5.956e1

InbreedingCoeff
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SIO_000300: -1.0e-4

DP
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SIO_000300: 2.348824e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.39e-1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.349e0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16492
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: 11550
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
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: 1.499835018148004e-5
allele num: 66674
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.232e0

VQSLOD
type: SiteQuality
SIO_000300: -9.083e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.213e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.926e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.39e-1

QD
type: SiteQuality
SIO_000300: 9.220000000000001e0

DP
type: SiteQuality
SIO_000300: 2.347431e6

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5001500150015e-5
allele num: 66660
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
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: 8592
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.670019074041963e-5
allele num: 11534
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.359999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
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SIO_000300: 2.98e0

MQRankSum
type: SiteQuality
SIO_000300: 2.22e-1

FS
type: SiteQuality
SIO_000300: 6.817e0

DP
type: SiteQuality
SIO_000300: 2.345643e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.26e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -9.369e-1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
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
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allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.163602513381429e-4
allele num: 8594
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66658
num of homozygotes: 0

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.026e0

MQRankSum
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SIO_000300: -4.07e-1

ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
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BaseQRankSum
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MQ
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SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.345625e6

GenotypeQuality
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variant carriers: 1

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
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Latino
type: Population
allele count: 1
allele frequency: 8.674531575294934e-5
allele num: 11528
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66612
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
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MQRankSum
type: SiteQuality
SIO_000300: -5.83e-1

MQ
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InbreedingCoeff
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VQSLOD
type: SiteQuality
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BaseQRankSum
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SIO_000300: 7.73e-1

FS
type: SiteQuality
SIO_000300: 5.73e-1

ReadPosRankSum
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SIO_000300: 5.669999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.342862e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.3e-1

QD
type: SiteQuality
SIO_000300: 1.231e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
type: Population
allele count: 804
allele frequency: 7.733743747595229e-2
allele num: 10396
num of homozygotes: 28

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
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Other
type: Population
allele count: 3
allele frequency: 3.303964757709251e-3
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 27
allele frequency: 2.342936480388754e-3
allele num: 11524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.051114181031894e-4
allele num: 66596
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.067961165048543e-5
allele num: 16480
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.325e0

InbreedingCoeff
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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ClippingRankSum
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QD
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SIO_000300: 1.412e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.12e0

VQSLOD
type: SiteQuality
SIO_000300: 4.42e0

DP
type: SiteQuality
SIO_000300: 2.340815e6

GenotypeQuality
all individuals: 362
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 912
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2625
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26659
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3380
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7652
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2178
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13899
bin: 9.75e1
variant carriers: 13

South Asian
type: Population
allele count: 13
allele frequency: 7.902735562310031e-4
allele num: 16450
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: 8570
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66462
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.851e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.2e-1

DP
type: SiteQuality
SIO_000300: 2.29684e6

VQSLOD
type: SiteQuality
SIO_000300: 9.49e-1

FS
type: SiteQuality
SIO_000300: 2.333e0

MQRankSum
type: SiteQuality
SIO_000300: 8.92e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

QD
type: SiteQuality
SIO_000300: 1.192e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-2

GenotypeQuality
all individuals: 3289
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 906
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 904
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508159140952553e-5
allele num: 66306
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.955e1

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

MQRankSum
type: SiteQuality
SIO_000300: 7.63e-1

DP
type: SiteQuality
SIO_000300: 2.269695e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.046e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.503e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.94e-1

GenotypeQuality
all individuals: 23366
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1580
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 849
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13882
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 40
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1282
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1446
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 884
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510391493475109e-5
allele num: 66208
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.641342074816814e-5
allele num: 10372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.484927687750479e-4
allele num: 11478
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.218175173589962e-4
allele num: 16418
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

FS
type: SiteQuality
SIO_000300: 2.166e0

QD
type: SiteQuality
SIO_000300: 1.27e1

DP
type: SiteQuality
SIO_000300: 2.243379e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.36e0

MQRankSum
type: SiteQuality
SIO_000300: -1.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e-2

GenotypeQuality
all individuals: 1303
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2414
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 884
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
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variant carriers: 0

GenotypeQuality
all individuals: 880
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variant carriers: 0

GenotypeQuality
all individuals: 55
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variant carriers: 0

GenotypeQuality
all individuals: 2073
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variant carriers: 0

GenotypeQuality
all individuals: 531
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variant carriers: 0

GenotypeQuality
all individuals: 3143
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variant carriers: 0

GenotypeQuality
all individuals: 1645
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13903
bin: 9.75e1
variant carriers: 41

GenotypeQuality
all individuals: 6894
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1276
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1578
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.643201542912247e-5
allele num: 10370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.26736803918012e-4
allele num: 66156
num of homozygotes: 0

East Asian
type: Population
allele count: 21
allele frequency: 2.467685076380728e-3
allele num: 8510
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.745200698080279e-4
allele num: 11460
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: 6552
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.219066195294405e-4
allele num: 16406
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.91e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e-2

DP
type: SiteQuality
SIO_000300: 2.237846e6

MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.845e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.19e-1

QD
type: SiteQuality
SIO_000300: 1.349e1

GenotypeQuality
all individuals: 5398
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2677
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13858
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variant carriers: 1

GenotypeQuality
all individuals: 18001
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variant carriers: 0

GenotypeQuality
all individuals: 1259
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variant carriers: 0

GenotypeQuality
all individuals: 2034
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variant carriers: 0

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
all individuals: 2960
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1463
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variant carriers: 0

GenotypeQuality
all individuals: 2886
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variant carriers: 0

GenotypeQuality
all individuals: 2115
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variant carriers: 0

GenotypeQuality
all individuals: 1699
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variant carriers: 0

GenotypeQuality
all individuals: 869
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variant carriers: 0

GenotypeQuality
all individuals: 890
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1270
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16392
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8500
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.652509652509652e-5
allele num: 10360
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66094
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

MQRankSum
type: SiteQuality
SIO_000300: 5.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.54e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.355e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.151e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.178879e6

GenotypeQuality
all individuals: 552
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4358
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variant carriers: 0

GenotypeQuality
all individuals: 3963
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variant carriers: 0

GenotypeQuality
all individuals: 1311
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
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variant carriers: 0

GenotypeQuality
all individuals: 1254
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variant carriers: 0

GenotypeQuality
all individuals: 964
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variant carriers: 0

GenotypeQuality
all individuals: 1449
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 338
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GenotypeQuality
all individuals: 21264
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variant carriers: 1

GenotypeQuality
all individuals: 3188
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variant carriers: 0

GenotypeQuality
all individuals: 5131
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GenotypeQuality
all individuals: 776
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variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2257
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3168
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7005
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16420
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.118568232662192e-3
allele num: 894
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64544
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8322
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9760
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e0

VQSLOD
type: SiteQuality
SIO_000300: -1.132e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.225943e6

MQ
type: SiteQuality
SIO_000300: 5.758e1

MQRankSum
type: SiteQuality
SIO_000300: 9.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.83e1

GenotypeQuality
all individuals: 21244
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1074
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 808
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3883
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variant carriers: 0

GenotypeQuality
all individuals: 988
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GenotypeQuality
all individuals: 7736
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GenotypeQuality
all individuals: 1292
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variant carriers: 0

GenotypeQuality
all individuals: 229
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GenotypeQuality
all individuals: 264
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variant carriers: 0

GenotypeQuality
all individuals: 1722
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variant carriers: 0

GenotypeQuality
all individuals: 217
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variant carriers: 0

GenotypeQuality
all individuals: 5144
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3101
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variant carriers: 0

GenotypeQuality
all individuals: 2235
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GenotypeQuality
all individuals: 3175
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GenotypeQuality
all individuals: 1258
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 444
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variant carriers: 0

GenotypeQuality
all individuals: 1343
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4246
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.551590380139643e-5
allele num: 64450
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11414
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16400
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8312
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.75e-1

MQ
type: SiteQuality
SIO_000300: 6.076e1

DP
type: SiteQuality
SIO_000300: 2.235808e6

VQSLOD
type: SiteQuality
SIO_000300: -2.038e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.906e0

MQRankSum
type: SiteQuality
SIO_000300: 3.26e-1

QD
type: SiteQuality
SIO_000300: 4.91e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

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

GenotypeQuality
all individuals: 3898
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variant carriers: 0

GenotypeQuality
all individuals: 5234
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2241
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GenotypeQuality
all individuals: 3185
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GenotypeQuality
all individuals: 200
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GenotypeQuality
all individuals: 838
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GenotypeQuality
all individuals: 961
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GenotypeQuality
all individuals: 235
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GenotypeQuality
all individuals: 1769
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GenotypeQuality
all individuals: 360
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GenotypeQuality
all individuals: 205
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GenotypeQuality
all individuals: 21245
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GenotypeQuality
all individuals: 8175
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GenotypeQuality
all individuals: 1248
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variant carriers: 0

GenotypeQuality
all individuals: 1313
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3125
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9772
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.55115716324378e-5
allele num: 64468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8322
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.051e1

DP
type: SiteQuality
SIO_000300: 2.242376e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.21e-1

QD
type: SiteQuality
SIO_000300: 1.33e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.446e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.74e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.54e0

FS
type: SiteQuality
SIO_000300: 1.2489e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

GenotypeQuality
all individuals: 603
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 766
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2298
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1122
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5431
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3238
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4314
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21295
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 218
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8722
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3940
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3229
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1050
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 879
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.551349674216568e-5
allele num: 64460
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9704
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8374
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.965e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e-1

MQ
type: SiteQuality
SIO_000300: 5.998e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.303159e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

QD
type: SiteQuality
SIO_000300: 4.72e0

GenotypeQuality
all individuals: 1521
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 917
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4066
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1224
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1214
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1234
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1200
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2174
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20879
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7249
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4916
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1193
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3762
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2977
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 837
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 933
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62730
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8350
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6426
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.197322756569162e-5
allele num: 16136
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11288
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

FS
type: SiteQuality
SIO_000300: 2.709e0

QD
type: SiteQuality
SIO_000300: 1.799e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e-1

DP
type: SiteQuality
SIO_000300: 2.395201e6

VQSLOD
type: SiteQuality
SIO_000300: -8.973e-1

MQ
type: SiteQuality
SIO_000300: 5.669e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.98e-1

GenotypeQuality
all individuals: 828
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 555
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3851
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 706
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 841
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4066
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4046
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27668
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2965
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4514
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2975
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4291
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16336
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.023122570083896e-4
allele num: 9774
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64970
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.876e1

VQSLOD
type: SiteQuality
SIO_000300: -5.365e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.467e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.042e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.241e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.18e-1

DP
type: SiteQuality
SIO_000300: 2.467268e6

FS
type: SiteQuality
SIO_000300: 8.627000000000001e0

QD
type: SiteQuality
SIO_000300: 5.600000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.0e-1

GenotypeQuality
all individuals: 549
bin: 2.25e1
variant carriers: 42

GenotypeQuality
all individuals: 263
bin: 1.75e1
variant carriers: 35

GenotypeQuality
all individuals: 418
bin: 2.5e0
variant carriers: 93

GenotypeQuality
all individuals: 293
bin: 7.5e0
variant carriers: 71

GenotypeQuality
all individuals: 4046
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4514
bin: 6.25e1
variant carriers: 5

GenotypeQuality
all individuals: 4291
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 4.25e1
variant carriers: 7

GenotypeQuality
all individuals: 255
bin: 1.25e1
variant carriers: 51

GenotypeQuality
all individuals: 586
bin: 3.75e1
variant carriers: 13

GenotypeQuality
all individuals: 3851
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 828
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 706
bin: 4.75e1
variant carriers: 5

GenotypeQuality
all individuals: 555
bin: 3.25e1
variant carriers: 17

GenotypeQuality
all individuals: 431
bin: 2.75e1
variant carriers: 19

GenotypeQuality
all individuals: 27668
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2965
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 841
bin: 5.25e1
variant carriers: 5

GenotypeQuality
all individuals: 2975
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.371354043158644e-4
allele num: 8434
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 9.208103130755065e-4
allele num: 9774
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.526717557251908e-4
allele num: 6550
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.224289911851126e-4
allele num: 16336
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.368338284116722e-4
allele num: 11446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 41
allele frequency: 6.310604894566723e-4
allele num: 64970
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.467e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.0e-1

DP
type: SiteQuality
SIO_000300: 2.467268e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.042e0

FS
type: SiteQuality
SIO_000300: 8.627000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.18e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.365e-1

MQ
type: SiteQuality
SIO_000300: 5.876e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.241e-1

QD
type: SiteQuality
SIO_000300: 5.600000000000001e-1

GenotypeQuality
all individuals: 3047
bin: 6.25e1
variant carriers: 535

GenotypeQuality
all individuals: 1806
bin: 1.25e1
variant carriers: 760

GenotypeQuality
all individuals: 1762
bin: 2.75e1
variant carriers: 705

GenotypeQuality
all individuals: 1476
bin: 5.25e1
variant carriers: 536

GenotypeQuality
all individuals: 2004
bin: 9.25e1
variant carriers: 336

GenotypeQuality
all individuals: 1985
bin: 7.5e0
variant carriers: 732

GenotypeQuality
all individuals: 6899
bin: 2.5e0
variant carriers: 736

GenotypeQuality
all individuals: 2028
bin: 8.25e1
variant carriers: 351

GenotypeQuality
all individuals: 1847
bin: 3.25e1
variant carriers: 723

GenotypeQuality
all individuals: 2222
bin: 6.75e1
variant carriers: 463

GenotypeQuality
all individuals: 2106
bin: 7.75e1
variant carriers: 404

GenotypeQuality
all individuals: 16263
bin: 9.75e1
variant carriers: 4258

GenotypeQuality
all individuals: 1713
bin: 3.75e1
variant carriers: 659

GenotypeQuality
all individuals: 1430
bin: 5.75e1
variant carriers: 510

GenotypeQuality
all individuals: 1548
bin: 4.75e1
variant carriers: 588

GenotypeQuality
all individuals: 1604
bin: 4.25e1
variant carriers: 656

GenotypeQuality
all individuals: 1778
bin: 7.25e1
variant carriers: 434

GenotypeQuality
all individuals: 1930
bin: 2.25e1
variant carriers: 695

GenotypeQuality
all individuals: 1509
bin: 8.75e1
variant carriers: 335

Latino
type: Population
allele count: 574
allele frequency: 6.161442679261486e-2
allele num: 9316
num of homozygotes: 6

South Asian
type: Population
allele count: 1274
allele frequency: 9.862207772100945e-2
allele num: 12918
num of homozygotes: 5

European (Finnish)
type: Population
allele count: 622
allele frequency: 1.335337054529841e-1
allele num: 4658
num of homozygotes: 2

Other
type: Population
allele count: 95
allele frequency: 1.405325443786982e-1
allele num: 676
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 8225
allele frequency: 1.75680293904054e-1
allele num: 46818
num of homozygotes: 111

East Asian
type: Population
allele count: 171
allele frequency: 2.332878581173261e-2
allele num: 7330
num of homozygotes: 2

African
type: Population
allele count: 1176
allele frequency: 1.987829614604462e-1
allele num: 5916
num of homozygotes: 24

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.98e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.5e-2

QD
type: SiteQuality
SIO_000300: 2.31e0

MQ
type: SiteQuality
SIO_000300: 5.798e1

FS
type: SiteQuality
SIO_000300: 5.305e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 2.397437e6

GenotypeQuality
all individuals: 6899
bin: 2.5e0
variant carriers: 444

GenotypeQuality
all individuals: 1899
bin: 1.75e1
variant carriers: 494

GenotypeQuality
all individuals: 1930
bin: 2.25e1
variant carriers: 460

GenotypeQuality
all individuals: 1762
bin: 2.75e1
variant carriers: 418

GenotypeQuality
all individuals: 2222
bin: 6.75e1
variant carriers: 228

GenotypeQuality
all individuals: 1430
bin: 5.75e1
variant carriers: 258

GenotypeQuality
all individuals: 1476
bin: 5.25e1
variant carriers: 306

GenotypeQuality
all individuals: 1847
bin: 3.25e1
variant carriers: 398

GenotypeQuality
all individuals: 1806
bin: 1.25e1
variant carriers: 510

GenotypeQuality
all individuals: 3047
bin: 6.25e1
variant carriers: 250

GenotypeQuality
all individuals: 1985
bin: 7.5e0
variant carriers: 579

GenotypeQuality
all individuals: 1713
bin: 3.75e1
variant carriers: 384

GenotypeQuality
all individuals: 1548
bin: 4.75e1
variant carriers: 331

GenotypeQuality
all individuals: 1509
bin: 8.75e1
variant carriers: 135

GenotypeQuality
all individuals: 16263
bin: 9.75e1
variant carriers: 1405

GenotypeQuality
all individuals: 2106
bin: 7.75e1
variant carriers: 183

GenotypeQuality
all individuals: 2028
bin: 8.25e1
variant carriers: 145

GenotypeQuality
all individuals: 2004
bin: 9.25e1
variant carriers: 140

GenotypeQuality
all individuals: 1778
bin: 7.25e1
variant carriers: 189

South Asian
type: Population
allele count: 849
allele frequency: 6.572224802601022e-2
allele num: 12918
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 3443
allele frequency: 7.354009141783074e-2
allele num: 46818
num of homozygotes: 19

European (Finnish)
type: Population
allele count: 214
allele frequency: 4.594246457707171e-2
allele num: 4658
num of homozygotes: 1

East Asian
type: Population
allele count: 51
allele frequency: 6.957708049113233e-3
allele num: 7330
num of homozygotes: 0

African
type: Population
allele count: 556
allele frequency: 9.398242055442867e-2
allele num: 5916
num of homozygotes: 3

Other
type: Population
allele count: 54
allele frequency: 7.988165680473373e-2
allele num: 676
num of homozygotes: 1

Latino
type: Population
allele count: 318
allele frequency: 3.413482181193645e-2
allele num: 9316
num of homozygotes: 2

DP
type: SiteQuality
SIO_000300: 2.397437e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

FS
type: SiteQuality
SIO_000300: 5.305e0

MQ
type: SiteQuality
SIO_000300: 5.798e1

MQRankSum
type: SiteQuality
SIO_000300: -3.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.5e-2

QD
type: SiteQuality
SIO_000300: 2.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.98e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.32e-1

GenotypeQuality
all individuals: 1476
bin: 5.25e1
variant carriers: 42

GenotypeQuality
all individuals: 2004
bin: 9.25e1
variant carriers: 21

GenotypeQuality
all individuals: 1604
bin: 4.25e1
variant carriers: 61

GenotypeQuality
all individuals: 6899
bin: 2.5e0
variant carriers: 229

GenotypeQuality
all individuals: 3047
bin: 6.25e1
variant carriers: 32

GenotypeQuality
all individuals: 1548
bin: 4.75e1
variant carriers: 71

GenotypeQuality
all individuals: 2106
bin: 7.75e1
variant carriers: 30

GenotypeQuality
all individuals: 1806
bin: 1.25e1
variant carriers: 108

GenotypeQuality
all individuals: 1713
bin: 3.75e1
variant carriers: 71

GenotypeQuality
all individuals: 16263
bin: 9.75e1
variant carriers: 273

GenotypeQuality
all individuals: 1930
bin: 2.25e1
variant carriers: 102

GenotypeQuality
all individuals: 1985
bin: 7.5e0
variant carriers: 105

GenotypeQuality
all individuals: 1847
bin: 3.25e1
variant carriers: 74

GenotypeQuality
all individuals: 1762
bin: 2.75e1
variant carriers: 91

GenotypeQuality
all individuals: 1509
bin: 8.75e1
variant carriers: 21

GenotypeQuality
all individuals: 2028
bin: 8.25e1
variant carriers: 29

GenotypeQuality
all individuals: 2222
bin: 6.75e1
variant carriers: 36

GenotypeQuality
all individuals: 1778
bin: 7.25e1
variant carriers: 27

GenotypeQuality
all individuals: 1430
bin: 5.75e1
variant carriers: 42

East Asian
type: Population
allele count: 18
allele frequency: 2.455661664392906e-3
allele num: 7330
num of homozygotes: 0

South Asian
type: Population
allele count: 145
allele frequency: 1.122464777829385e-2
allele num: 12918
num of homozygotes: 3

European (Finnish)
type: Population
allele count: 22
allele frequency: 4.723057106054101e-3
allele num: 4658
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 573
allele frequency: 1.223888248109701e-2
allele num: 46818
num of homozygotes: 1

Latino
type: Population
allele count: 86
allele frequency: 9.23142979819665e-3
allele num: 9316
num of homozygotes: 1

Other
type: Population
allele count: 7
allele frequency: 1.035502958579882e-2
allele num: 676
num of homozygotes: 1

African
type: Population
allele count: 144
allele frequency: 2.434077079107505e-2
allele num: 5916
num of homozygotes: 1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.5e-2

DP
type: SiteQuality
SIO_000300: 2.397437e6

MQRankSum
type: SiteQuality
SIO_000300: -3.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.98e-2

QD
type: SiteQuality
SIO_000300: 2.31e0

MQ
type: SiteQuality
SIO_000300: 5.798e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.19e-1

FS
type: SiteQuality
SIO_000300: 5.305e0

VQSLOD
type: SiteQuality
SIO_000300: 3.32e-1

GenotypeQuality
all individuals: 2004
bin: 9.25e1
variant carriers: 6

GenotypeQuality
all individuals: 1430
bin: 5.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1985
bin: 7.5e0
variant carriers: 10

GenotypeQuality
all individuals: 1806
bin: 1.25e1
variant carriers: 15

GenotypeQuality
all individuals: 1778
bin: 7.25e1
variant carriers: 6

GenotypeQuality
all individuals: 1930
bin: 2.25e1
variant carriers: 10

GenotypeQuality
all individuals: 1604
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 6899
bin: 2.5e0
variant carriers: 52

GenotypeQuality
all individuals: 2222
bin: 6.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1713
bin: 3.75e1
variant carriers: 8

GenotypeQuality
all individuals: 16263
bin: 9.75e1
variant carriers: 34

GenotypeQuality
all individuals: 2106
bin: 7.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1476
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1899
bin: 1.75e1
variant carriers: 18

GenotypeQuality
all individuals: 1548
bin: 4.75e1
variant carriers: 8

GenotypeQuality
all individuals: 2028
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1509
bin: 8.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1762
bin: 2.75e1
variant carriers: 10

GenotypeQuality
all individuals: 3047
bin: 6.25e1
variant carriers: 1

Other
type: Population
allele count: 1
allele frequency: 1.479289940828402e-3
allele num: 676
num of homozygotes: 0

South Asian
type: Population
allele count: 11
allele frequency: 8.515250038705681e-4
allele num: 12918
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.364256480218281e-4
allele num: 7330
num of homozygotes: 0

African
type: Population
allele count: 32
allele frequency: 5.409060175794456e-3
allele num: 5916
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 1.07342206955775e-3
allele num: 9316
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 53
allele frequency: 1.132043231235849e-3
allele num: 46818
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4658
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.98e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.14e-1

MQ
type: SiteQuality
SIO_000300: 5.798e1

QD
type: SiteQuality
SIO_000300: 2.31e0

FS
type: SiteQuality
SIO_000300: 5.305e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.5e-2

DP
type: SiteQuality
SIO_000300: 2.397437e6

VQSLOD
type: SiteQuality
SIO_000300: 3.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.19e-1

GenotypeQuality
all individuals: 1985
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 1548
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1509
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1762
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6899
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 16263
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1713
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1806
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2222
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1899
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1476
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1930
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1847
bin: 3.25e1
variant carriers: 3

GenotypeQuality
all individuals: 2028
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3047
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1604
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2106
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1778
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2004
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 6
allele frequency: 1.01419878296146e-3
allele num: 5916
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7330
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.1468441391155e-4
allele num: 9316
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.495151437481311e-4
allele num: 46818
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 676
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12918
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4658
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.798e1

DP
type: SiteQuality
SIO_000300: 2.397437e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.98e-2

QD
type: SiteQuality
SIO_000300: 2.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.5e-2

FS
type: SiteQuality
SIO_000300: 5.305e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

MQRankSum
type: SiteQuality
SIO_000300: -3.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.32e-1

GenotypeQuality
all individuals: 1713
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1548
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2106
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1806
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1604
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1847
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1930
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3047
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6899
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2028
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1899
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1476
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1985
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16263
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 1430
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1509
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1778
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2004
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2222
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.06796531248665e-4
allele num: 46818
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9316
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.364256480218281e-4
allele num: 7330
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4658
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 1.01419878296146e-3
allele num: 5916
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 3.096454559529339e-4
allele num: 12918
num of homozygotes: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 676
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.798e1

VQSLOD
type: SiteQuality
SIO_000300: 3.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.98e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.19e-1

QD
type: SiteQuality
SIO_000300: 2.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.5e-2

FS
type: SiteQuality
SIO_000300: 5.305e0

DP
type: SiteQuality
SIO_000300: 2.397437e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

GenotypeQuality
all individuals: 331
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1337
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1306
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10062
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 261
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 353
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1337
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 275
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2105
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1302
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 885
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 370
bin: 3.25e1
variant carriers: 1

South Asian
type: Population
allele count: 1
allele frequency: 1.198178768272226e-4
allele num: 8346
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 318
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 5.524861878453039e-4
allele num: 1810
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.140641040264629e-4
allele num: 17534
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.580777742649384e-4
allele num: 6326
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2288
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.490312965722802e-4
allele num: 6710
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.774e1

VQSLOD
type: SiteQuality
SIO_000300: -6.464e-1

FS
type: SiteQuality
SIO_000300: 4.964e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.0e-1

DP
type: SiteQuality
SIO_000300: 1.890151e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.56e-2

QD
type: SiteQuality
SIO_000300: 3.5e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.996e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.899999999999999e-1

GenotypeQuality
all individuals: 365
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1844
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3426
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 565
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1187
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 12875
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 291
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1917
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2667
bin: 6.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1800
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1846
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.865532422953511e-4
allele num: 26802
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6780
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9680
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7524
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 442
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3318
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.782e1

DP
type: SiteQuality
SIO_000300: 1.917327e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.02e-2

VQSLOD
type: SiteQuality
SIO_000300: -4.129e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.169999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.28e0

MQRankSum
type: SiteQuality
SIO_000300: -1.701e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.01e-1

QD
type: SiteQuality
SIO_000300: 4.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.53e-1

GenotypeQuality
all individuals: 1800
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 565
bin: 2.25e1
variant carriers: 13

GenotypeQuality
all individuals: 12875
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 475
bin: 3.75e1
variant carriers: 6

GenotypeQuality
all individuals: 572
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1846
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 258
bin: 1.75e1
variant carriers: 13

GenotypeQuality
all individuals: 3426
bin: 2.5e0
variant carriers: 15

GenotypeQuality
all individuals: 1844
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 297
bin: 1.25e1
variant carriers: 15

GenotypeQuality
all individuals: 1280
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 365
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 469
bin: 3.25e1
variant carriers: 11

GenotypeQuality
all individuals: 2667
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 1187
bin: 8.75e1
variant carriers: 4

GenotypeQuality
all individuals: 488
bin: 4.75e1
variant carriers: 9

GenotypeQuality
all individuals: 1917
bin: 7.75e1
variant carriers: 3

GenotypeQuality
all individuals: 391
bin: 2.75e1
variant carriers: 9

GenotypeQuality
all individuals: 424
bin: 4.25e1
variant carriers: 7

European (Non-Finnish)
type: Population
allele count: 53
allele frequency: 1.977464368330722e-3
allele num: 26802
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 3.013863773357444e-4
allele num: 3318
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 442
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.949852507374631e-4
allele num: 6780
num of homozygotes: 0

African
type: Population
allele count: 24
allele frequency: 6.798866855524079e-3
allele num: 3530
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.658160552897395e-4
allele num: 7524
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 4.132231404958678e-4
allele num: 9680
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.701e0

QD
type: SiteQuality
SIO_000300: 4.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.53e-1

MQ
type: SiteQuality
SIO_000300: 5.782e1

VQSLOD
type: SiteQuality
SIO_000300: -4.129e-1

DP
type: SiteQuality
SIO_000300: 1.917327e6

FS
type: SiteQuality
SIO_000300: 1.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.02e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.169999999999999e-1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6966
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5294
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.210067763794773e-4
allele num: 33056
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.284e0

MQ
type: SiteQuality
SIO_000300: 5.747e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.1e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.588e0

DP
type: SiteQuality
SIO_000300: 1.928574e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.54e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.65e-1

QD
type: SiteQuality
SIO_000300: 7.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

GenotypeQuality
all individuals: 187
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1572
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 345
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15498
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2379
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2307
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2399
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1499
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2215
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6966
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5294
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4016
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.025169409486931e-5
allele num: 33056
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7990
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 508
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.4e-1

FS
type: SiteQuality
SIO_000300: 1.284e0

VQSLOD
type: SiteQuality
SIO_000300: -5.99e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.588e0

MQ
type: SiteQuality
SIO_000300: 5.747e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.54e-1

DP
type: SiteQuality
SIO_000300: 1.928574e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.1e-1

GenotypeQuality
all individuals: 2215
bin: 6.75e1
variant carriers: 22

GenotypeQuality
all individuals: 494
bin: 2.25e1
variant carriers: 53

GenotypeQuality
all individuals: 224
bin: 1.75e1
variant carriers: 72

GenotypeQuality
all individuals: 427
bin: 4.75e1
variant carriers: 31

GenotypeQuality
all individuals: 381
bin: 3.25e1
variant carriers: 49

GenotypeQuality
all individuals: 392
bin: 3.75e1
variant carriers: 32

GenotypeQuality
all individuals: 15498
bin: 9.75e1
variant carriers: 61

GenotypeQuality
all individuals: 3033
bin: 6.25e1
variant carriers: 24

GenotypeQuality
all individuals: 187
bin: 1.25e1
variant carriers: 63

GenotypeQuality
all individuals: 209
bin: 7.5e0
variant carriers: 69

GenotypeQuality
all individuals: 345
bin: 4.25e1
variant carriers: 45

GenotypeQuality
all individuals: 282
bin: 2.5e0
variant carriers: 73

GenotypeQuality
all individuals: 2379
bin: 8.25e1
variant carriers: 9

GenotypeQuality
all individuals: 1572
bin: 7.25e1
variant carriers: 22

GenotypeQuality
all individuals: 315
bin: 2.75e1
variant carriers: 42

GenotypeQuality
all individuals: 494
bin: 5.25e1
variant carriers: 19

GenotypeQuality
all individuals: 1499
bin: 8.75e1
variant carriers: 12

GenotypeQuality
all individuals: 2399
bin: 7.75e1
variant carriers: 18

GenotypeQuality
all individuals: 385
bin: 5.75e1
variant carriers: 30

African
type: Population
allele count: 77
allele frequency: 1.454476766150359e-2
allele num: 5294
num of homozygotes: 0

Latino
type: Population
allele count: 26
allele frequency: 3.254067584480601e-3
allele num: 7990
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 1.00488084984209e-3
allele num: 6966
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 316
allele frequency: 9.559535333978703e-3
allele num: 33056
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 14
allele frequency: 3.48605577689243e-3
allele num: 4016
num of homozygotes: 0

South Asian
type: Population
allele count: 36
allele frequency: 3.535651149086624e-3
allele num: 10182
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 5.905511811023622e-3
allele num: 508
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.54e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.588e0

FS
type: SiteQuality
SIO_000300: 1.284e0

DP
type: SiteQuality
SIO_000300: 1.928574e6

MQ
type: SiteQuality
SIO_000300: 5.747e1

VQSLOD
type: SiteQuality
SIO_000300: -5.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.1e-1

QD
type: SiteQuality
SIO_000300: 7.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.65e-1

GenotypeQuality
all individuals: 579
bin: 1.25e1
variant carriers: 218

GenotypeQuality
all individuals: 735
bin: 2.5e0
variant carriers: 259

GenotypeQuality
all individuals: 2079
bin: 9.25e1
variant carriers: 35

GenotypeQuality
all individuals: 1555
bin: 7.25e1
variant carriers: 56

GenotypeQuality
all individuals: 2987
bin: 6.25e1
variant carriers: 68

GenotypeQuality
all individuals: 2113
bin: 7.75e1
variant carriers: 58

GenotypeQuality
all individuals: 643
bin: 4.75e1
variant carriers: 112

GenotypeQuality
all individuals: 550
bin: 5.75e1
variant carriers: 84

GenotypeQuality
all individuals: 816
bin: 2.25e1
variant carriers: 188

GenotypeQuality
all individuals: 740
bin: 3.25e1
variant carriers: 159

GenotypeQuality
all individuals: 659
bin: 7.5e0
variant carriers: 280

GenotypeQuality
all individuals: 718
bin: 2.75e1
variant carriers: 199

GenotypeQuality
all individuals: 753
bin: 5.25e1
variant carriers: 108

GenotypeQuality
all individuals: 14929
bin: 9.75e1
variant carriers: 277

GenotypeQuality
all individuals: 760
bin: 3.75e1
variant carriers: 140

GenotypeQuality
all individuals: 1457
bin: 8.75e1
variant carriers: 46

GenotypeQuality
all individuals: 2084
bin: 8.25e1
variant carriers: 39

GenotypeQuality
all individuals: 607
bin: 1.75e1
variant carriers: 198

GenotypeQuality
all individuals: 664
bin: 4.25e1
variant carriers: 126

South Asian
type: Population
allele count: 114
allele frequency: 1.098689282960678e-2
allele num: 10376
num of homozygotes: 1

African
type: Population
allele count: 355
allele frequency: 6.610800744878957e-2
allele num: 5370
num of homozygotes: 0

Other
type: Population
allele count: 12
allele frequency: 2.298850574712644e-2
allele num: 522
num of homozygotes: 0

East Asian
type: Population
allele count: 27
allele frequency: 3.850541928123217e-3
allele num: 7012
num of homozygotes: 0

Latino
type: Population
allele count: 69
allele frequency: 8.597059556441565e-3
allele num: 8026
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 99
allele frequency: 2.368421052631579e-2
allele num: 4180
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 1061
allele frequency: 3.113445624743236e-2
allele num: 34078
num of homozygotes: 1

VQSLOD
type: SiteQuality
SIO_000300: -2.552e-1

DP
type: SiteQuality
SIO_000300: 1.925691e6

FS
type: SiteQuality
SIO_000300: 2.722e0

MQRankSum
type: SiteQuality
SIO_000300: -7.01e-1

MQ
type: SiteQuality
SIO_000300: 5.787e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.61e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.69e-1

QD
type: SiteQuality
SIO_000300: 1.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.26e-1

GenotypeQuality
all individuals: 1250
bin: 1.25e1
variant carriers: 557

GenotypeQuality
all individuals: 1311
bin: 2.25e1
variant carriers: 481

GenotypeQuality
all individuals: 1722
bin: 9.25e1
variant carriers: 97

GenotypeQuality
all individuals: 1282
bin: 7.5e0
variant carriers: 591

GenotypeQuality
all individuals: 1002
bin: 4.75e1
variant carriers: 314

GenotypeQuality
all individuals: 1109
bin: 4.25e1
variant carriers: 387

GenotypeQuality
all individuals: 977
bin: 5.25e1
variant carriers: 304

GenotypeQuality
all individuals: 1097
bin: 3.75e1
variant carriers: 376

GenotypeQuality
all individuals: 1326
bin: 8.75e1
variant carriers: 119

GenotypeQuality
all individuals: 2553
bin: 6.25e1
variant carriers: 248

GenotypeQuality
all individuals: 1735
bin: 7.75e1
variant carriers: 171

GenotypeQuality
all individuals: 13462
bin: 9.75e1
variant carriers: 1043

GenotypeQuality
all individuals: 3562
bin: 2.5e0
variant carriers: 535

GenotypeQuality
all individuals: 1199
bin: 3.25e1
variant carriers: 452

GenotypeQuality
all individuals: 878
bin: 5.75e1
variant carriers: 248

GenotypeQuality
all individuals: 1328
bin: 1.75e1
variant carriers: 591

GenotypeQuality
all individuals: 1801
bin: 6.75e1
variant carriers: 209

GenotypeQuality
all individuals: 1382
bin: 7.25e1
variant carriers: 163

GenotypeQuality
all individuals: 1774
bin: 8.25e1
variant carriers: 144

African
type: Population
allele count: 837
allele frequency: 1.636043784206411e-1
allele num: 5116
num of homozygotes: 9

Other
type: Population
allele count: 49
allele frequency: 8.90909090909091e-2
allele num: 550
num of homozygotes: 2

South Asian
type: Population
allele count: 306
allele frequency: 2.962245885769603e-2
allele num: 10330
num of homozygotes: 2

East Asian
type: Population
allele count: 71
allele frequency: 1.020408163265306e-2
allele num: 6958
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3443
allele frequency: 1.006960692559663e-1
allele num: 34192
num of homozygotes: 29

European (Finnish)
type: Population
allele count: 296
allele frequency: 7.007575757575757e-2
allele num: 4224
num of homozygotes: 1

Latino
type: Population
allele count: 221
allele frequency: 2.93804839138527e-2
allele num: 7522
num of homozygotes: 4

VQSLOD
type: SiteQuality
SIO_000300: 8.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.03e-1

FS
type: SiteQuality
SIO_000300: 2.777e0

QD
type: SiteQuality
SIO_000300: 1.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.69e-2

DP
type: SiteQuality
SIO_000300: 1.970919e6

MQRankSum
type: SiteQuality
SIO_000300: 9.2e-2

MQ
type: SiteQuality
SIO_000300: 5.823e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.8e-2

GenotypeQuality
all individuals: 1301
bin: 5.75e1
variant carriers: 629

GenotypeQuality
all individuals: 1387
bin: 4.75e1
variant carriers: 637

GenotypeQuality
all individuals: 1493
bin: 3.75e1
variant carriers: 579

GenotypeQuality
all individuals: 904
bin: 9.25e1
variant carriers: 575

GenotypeQuality
all individuals: 1400
bin: 4.25e1
variant carriers: 629

GenotypeQuality
all individuals: 2500
bin: 2.5e0
variant carriers: 465

GenotypeQuality
all individuals: 1722
bin: 2.25e1
variant carriers: 589

GenotypeQuality
all individuals: 1704
bin: 1.75e1
variant carriers: 516

GenotypeQuality
all individuals: 1257
bin: 6.25e1
variant carriers: 606

GenotypeQuality
all individuals: 1638
bin: 2.75e1
variant carriers: 584

GenotypeQuality
all individuals: 1080
bin: 7.75e1
variant carriers: 625

GenotypeQuality
all individuals: 1597
bin: 3.25e1
variant carriers: 637

GenotypeQuality
all individuals: 1059
bin: 7.25e1
variant carriers: 562

GenotypeQuality
all individuals: 1817
bin: 7.5e0
variant carriers: 532

GenotypeQuality
all individuals: 32988
bin: 9.75e1
variant carriers: 29385

GenotypeQuality
all individuals: 1251
bin: 5.25e1
variant carriers: 600

GenotypeQuality
all individuals: 1205
bin: 6.75e1
variant carriers: 649

GenotypeQuality
all individuals: 983
bin: 8.75e1
variant carriers: 572

GenotypeQuality
all individuals: 940
bin: 8.25e1
variant carriers: 545

South Asian
type: Population
allele count: 5087
allele frequency: 3.550886500069803e-1
allele num: 14326
num of homozygotes: 437

African
type: Population
allele count: 4082
allele frequency: 4.695192086496434e-1
allele num: 8694
num of homozygotes: 361

European (Non-Finnish)
type: Population
allele count: 25737
allele frequency: 4.430538819073851e-1
allele num: 58090
num of homozygotes: 1867

East Asian
type: Population
allele count: 983
allele frequency: 1.466288782816229e-1
allele num: 6704
num of homozygotes: 7

European (Finnish)
type: Population
allele count: 2313
allele frequency: 3.971497252747253e-1
allele num: 5824
num of homozygotes: 59

Latino
type: Population
allele count: 2491
allele frequency: 2.656216677329921e-1
allele num: 9378
num of homozygotes: 109

Other
type: Population
allele count: 334
allele frequency: 4.164588528678304e-1
allele num: 802
num of homozygotes: 29

MQ
type: SiteQuality
SIO_000300: 5.899e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.438e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.588000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.884963e6

MQRankSum
type: SiteQuality
SIO_000300: 4.01e-1

QD
type: SiteQuality
SIO_000300: 7.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.93e-1

FS
type: SiteQuality
SIO_000300: 9.581e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.66e-1

GenotypeQuality
all individuals: 1251
bin: 5.25e1
variant carriers: 137

GenotypeQuality
all individuals: 1493
bin: 3.75e1
variant carriers: 184

GenotypeQuality
all individuals: 1205
bin: 6.75e1
variant carriers: 120

GenotypeQuality
all individuals: 1771
bin: 1.25e1
variant carriers: 289

GenotypeQuality
all individuals: 1704
bin: 1.75e1
variant carriers: 249

GenotypeQuality
all individuals: 1257
bin: 6.25e1
variant carriers: 129

GenotypeQuality
all individuals: 1638
bin: 2.75e1
variant carriers: 218

GenotypeQuality
all individuals: 1059
bin: 7.25e1
variant carriers: 113

GenotypeQuality
all individuals: 2500
bin: 2.5e0
variant carriers: 246

GenotypeQuality
all individuals: 1817
bin: 7.5e0
variant carriers: 259

GenotypeQuality
all individuals: 940
bin: 8.25e1
variant carriers: 93

GenotypeQuality
all individuals: 1301
bin: 5.75e1
variant carriers: 142

GenotypeQuality
all individuals: 1400
bin: 4.25e1
variant carriers: 169

GenotypeQuality
all individuals: 983
bin: 8.75e1
variant carriers: 81

GenotypeQuality
all individuals: 1387
bin: 4.75e1
variant carriers: 140

GenotypeQuality
all individuals: 1722
bin: 2.25e1
variant carriers: 256

GenotypeQuality
all individuals: 1597
bin: 3.25e1
variant carriers: 194

GenotypeQuality
all individuals: 32988
bin: 9.75e1
variant carriers: 964

GenotypeQuality
all individuals: 904
bin: 9.25e1
variant carriers: 64

Other
type: Population
allele count: 26
allele frequency: 3.241895261845387e-2
allele num: 802
num of homozygotes: 0

South Asian
type: Population
allele count: 1080
allele frequency: 7.538740751081949e-2
allele num: 14326
num of homozygotes: 0

Latino
type: Population
allele count: 610
allele frequency: 6.504585199402858e-2
allele num: 9378
num of homozygotes: 0

East Asian
type: Population
allele count: 395
allele frequency: 5.89200477326969e-2
allele num: 6704
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 892
allele frequency: 1.535548287140644e-2
allele num: 58090
num of homozygotes: 0

African
type: Population
allele count: 65
allele frequency: 7.47642051989878e-3
allele num: 8694
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 47
allele frequency: 8.070054945054946e-3
allele num: 5824
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.438e-1

DP
type: SiteQuality
SIO_000300: 2.884963e6

VQSLOD
type: SiteQuality
SIO_000300: -6.588000000000001e-1

FS
type: SiteQuality
SIO_000300: 9.581e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.66e-1

MQ
type: SiteQuality
SIO_000300: 5.899e1

QD
type: SiteQuality
SIO_000300: 7.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQRankSum
type: SiteQuality
SIO_000300: 4.01e-1

GenotypeQuality
all individuals: 940
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1704
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1722
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1251
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1638
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 983
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1771
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 904
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1400
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2500
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 1817
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 1257
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1080
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1387
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1493
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1597
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32988
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1301
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1059
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8694
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.032880013771734e-4
allele num: 58090
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.717032967032967e-4
allele num: 5824
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.983293556085919e-4
allele num: 6704
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.094094653078319e-4
allele num: 14326
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.66e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.01e-1

QD
type: SiteQuality
SIO_000300: 7.92e0

FS
type: SiteQuality
SIO_000300: 9.581e0

MQ
type: SiteQuality
SIO_000300: 5.899e1

VQSLOD
type: SiteQuality
SIO_000300: -6.588000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.438e-1

DP
type: SiteQuality
SIO_000300: 2.884963e6

GenotypeQuality
all individuals: 1080
bin: 7.75e1
variant carriers: 219

GenotypeQuality
all individuals: 983
bin: 8.75e1
variant carriers: 223

GenotypeQuality
all individuals: 32988
bin: 9.75e1
variant carriers: 2382

GenotypeQuality
all individuals: 1301
bin: 5.75e1
variant carriers: 307

GenotypeQuality
all individuals: 1771
bin: 1.25e1
variant carriers: 353

GenotypeQuality
all individuals: 2500
bin: 2.5e0
variant carriers: 372

GenotypeQuality
all individuals: 1257
bin: 6.25e1
variant carriers: 317

GenotypeQuality
all individuals: 1704
bin: 1.75e1
variant carriers: 408

GenotypeQuality
all individuals: 1400
bin: 4.25e1
variant carriers: 308

GenotypeQuality
all individuals: 940
bin: 8.25e1
variant carriers: 212

GenotypeQuality
all individuals: 1638
bin: 2.75e1
variant carriers: 413

GenotypeQuality
all individuals: 1817
bin: 7.5e0
variant carriers: 411

GenotypeQuality
all individuals: 1205
bin: 6.75e1
variant carriers: 275

GenotypeQuality
all individuals: 1722
bin: 2.25e1
variant carriers: 414

GenotypeQuality
all individuals: 1597
bin: 3.25e1
variant carriers: 369

GenotypeQuality
all individuals: 1059
bin: 7.25e1
variant carriers: 231

GenotypeQuality
all individuals: 1387
bin: 4.75e1
variant carriers: 329

GenotypeQuality
all individuals: 1251
bin: 5.25e1
variant carriers: 268

GenotypeQuality
all individuals: 904
bin: 9.25e1
variant carriers: 195

Latino
type: Population
allele count: 1132
allele frequency: 1.207080400938366e-1
allele num: 9378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2591
allele frequency: 4.460320192804269e-2
allele num: 58090
num of homozygotes: 0

South Asian
type: Population
allele count: 1058
allele frequency: 7.385173809856206e-2
allele num: 14326
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 303
allele frequency: 5.20260989010989e-2
allele num: 5824
num of homozygotes: 0

Other
type: Population
allele count: 51
allele frequency: 6.359102244389027e-2
allele num: 802
num of homozygotes: 0

African
type: Population
allele count: 201
allele frequency: 2.311939268461008e-2
allele num: 8694
num of homozygotes: 0

East Asian
type: Population
allele count: 1477
allele frequency: 2.203162291169451e-1
allele num: 6704
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.899e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQRankSum
type: SiteQuality
SIO_000300: 4.01e-1

DP
type: SiteQuality
SIO_000300: 2.884963e6

FS
type: SiteQuality
SIO_000300: 9.581e0

VQSLOD
type: SiteQuality
SIO_000300: -6.588000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.93e-1

QD
type: SiteQuality
SIO_000300: 7.92e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.438e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.66e-1

East Asian
type: Population
allele count: 8
allele frequency: 1.193317422434368e-3
allele num: 6704
num of homozygotes: 0

Latino
type: Population
allele count: 15
allele frequency: 1.599488163787588e-3
allele num: 9378
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 6.980315510261064e-4
allele num: 14326
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.92e0

VQSLOD
type: SiteQuality
SIO_000300: -6.588000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.01e-1

FS
type: SiteQuality
SIO_000300: 9.581e0

MQ
type: SiteQuality
SIO_000300: 5.899e1

DP
type: SiteQuality
SIO_000300: 2.884963e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.438e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

GenotypeQuality
all individuals: 113
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 200
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 1.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1412
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 114
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 80
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.627462014631402e-4
allele num: 3554
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 76
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.24e0

MQRankSum
type: SiteQuality
SIO_000300: -7.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.106e-1

DP
type: SiteQuality
SIO_000300: 1.54271e6

QD
type: SiteQuality
SIO_000300: 8.51e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

FS
type: SiteQuality
SIO_000300: 1.827e0

GenotypeQuality
all individuals: 615
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 416
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66326
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e0

MQRankSum
type: SiteQuality
SIO_000300: -1.343e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.43e0

DP
type: SiteQuality
SIO_000300: 3.500919e6

MQ
type: SiteQuality
SIO_000300: 6.089e1

FS
type: SiteQuality
SIO_000300: 7.619e0

ClippingRankSum
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SIO_000300: -4.733e0

BaseQRankSum
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SIO_000300: -6.798e0

QD
type: SiteQuality
SIO_000300: 1.188e1

GenotypeQuality
all individuals: 242
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3487
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GenotypeQuality
all individuals: 3661
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.514954759972345e-5
allele num: 66534
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.67305088024763e-5
allele num: 10338
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
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: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 5.815e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.63e-1

MQ
type: SiteQuality
SIO_000300: 5.69e1

BaseQRankSum
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SIO_000300: 6.6e-2

MQRankSum
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SIO_000300: -4.11e-1

DP
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SIO_000300: 3.526252e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 6.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.53e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.806e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 8

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 656
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 3003
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GenotypeQuality
all individuals: 628
bin: 5.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6424
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.906280327187023e-4
allele num: 57704
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.232134056185313e-4
allele num: 8116
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.473285335354301e-5
allele num: 10556
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.013693113169553e-4
allele num: 14898
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 758
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.411e0

MQ
type: SiteQuality
SIO_000300: 5.788e1

VQSLOD
type: SiteQuality
SIO_000300: -2.416e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e0

DP
type: SiteQuality
SIO_000300: 3.632178e6

MQRankSum
type: SiteQuality
SIO_000300: -2.6e-1

FS
type: SiteQuality
SIO_000300: 2.0237e1

QD
type: SiteQuality
SIO_000300: 2.63e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
all individuals: 27514
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variant carriers: 1

GenotypeQuality
all individuals: 4339
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10556
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.232134056185313e-4
allele num: 8116
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 758
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.732982115624567e-5
allele num: 57704
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6424
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14898
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.411e0

FS
type: SiteQuality
SIO_000300: 2.0237e1

MQRankSum
type: SiteQuality
SIO_000300: -2.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-2

ReadPosRankSum
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.788e1

DP
type: SiteQuality
SIO_000300: 3.632178e6

VQSLOD
type: SiteQuality
SIO_000300: -2.416e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e0

QD
type: SiteQuality
SIO_000300: 2.63e0

GenotypeDepth
all individuals: 5474
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variant carriers: 683

GenotypeDepth
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variant carriers: 599

GenotypeQuality
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variant carriers: 398

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 371

GenotypeQuality
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variant carriers: 2097

GenotypeQuality
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bin: 2.25e1
variant carriers: 378

GenotypeQuality
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variant carriers: 220

GenotypeQuality
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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: 259

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 313

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 388

GenotypeQuality
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variant carriers: 209

GenotypeQuality
all individuals: 1159
bin: 4.25e1
variant carriers: 342

GenotypeQuality
all individuals: 2353
bin: 7.25e1
variant carriers: 232

South Asian
type: Population
allele count: 677
allele frequency: 4.448679195689315e-2
allele num: 15218
num of homozygotes: 0

Other
type: Population
allele count: 49
allele frequency: 6.109725685785536e-2
allele num: 802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3912
allele frequency: 6.668939652233208e-2
allele num: 58660
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 363
allele frequency: 6.033909574468085e-2
allele num: 6016
num of homozygotes: 0

East Asian
type: Population
allele count: 64
allele frequency: 7.620862110026196e-3
allele num: 8398
num of homozygotes: 0

Latino
type: Population
allele count: 220
allele frequency: 2.018348623853211e-2
allele num: 10900
num of homozygotes: 0

African
type: Population
allele count: 953
allele frequency: 1.123820754716981e-1
allele num: 8480
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.41e0

DP
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MQ
type: SiteQuality
SIO_000300: 5.746e1

MQRankSum
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FS
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SIO_000300: 4.134e1

QD
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.319e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.81e-2

VQSLOD
type: SiteQuality
SIO_000300: -7.97e0

GenotypeDepth
all individuals: 5151
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2909
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GenotypeQuality
all individuals: 3683
bin: 6.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66716
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 8.24e0

FS
type: SiteQuality
SIO_000300: 1.0969e1

DP
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SIO_000300: 3.692452e6

MQ
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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VQSLOD
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SIO_000300: -1.491e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.08e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 29
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GenotypeQuality
all individuals: 51
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

South Asian
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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: 1.498666187093487e-5
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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MQRankSum
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SIO_000300: -5.6e-2

ReadPosRankSum
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FS
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ClippingRankSum
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DP
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InbreedingCoeff
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BaseQRankSum
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QD
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VQSLOD
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MQ
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

South Asian
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Other
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Latino
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African
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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FS
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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DP
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MQ
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VQSLOD
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ClippingRankSum
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QD
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GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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allele num: 902
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Latino
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European (Finnish)
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allele frequency: 3.158559696778269e-3
allele num: 6332
num of homozygotes: 0

African
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.00147072065312e-5
allele num: 66634
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FS
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VQSLOD
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QD
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DP
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ClippingRankSum
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MQ
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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SIO_000300: -1.1e-3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

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

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

African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
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East Asian
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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QD
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SIO_000300: 2.982e1

ReadPosRankSum
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ClippingRankSum
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FS
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VQSLOD
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MQ
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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DP
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SIO_000300: 3.692335e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 11578
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 1.388888888888889e-3
allele num: 6480
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African
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Other
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.499160470136723e-5
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ClippingRankSum
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MQ
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DP
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QD
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ReadPosRankSum
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MQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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European (Non-Finnish)
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Latino
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African
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East Asian
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European (Finnish)
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allele frequency: 1.249609497032177e-3
allele num: 6402
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InbreedingCoeff
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FS
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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QD
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DP
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

European (Non-Finnish)
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Other
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Latino
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African
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East Asian
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European (Finnish)
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FS
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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QD
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BaseQRankSum
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MQRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
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num of homozygotes: 0

European (Finnish)
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European (Non-Finnish)
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African
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Other
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South Asian
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East Asian
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MQRankSum
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FS
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InbreedingCoeff
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MQ
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ReadPosRankSum
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DP
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BaseQRankSum
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VQSLOD
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QD
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ClippingRankSum
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SIO_000300: -4.61e-1

GenotypeQuality
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variant carriers: 1

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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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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allele num: 16512
num of homozygotes: 0

European (Finnish)
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allele count: 0
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num of homozygotes: 0

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

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

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

European (Non-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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num of homozygotes: 0

South Asian
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allele num: 16512
num of homozygotes: 0

Latino
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num of homozygotes: 0

MQRankSum
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SIO_000300: -2.2e-1

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

Latino
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allele num: 11576
num of homozygotes: 0

African
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num of homozygotes: 0

European (Finnish)
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Other
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num of homozygotes: 0

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

Latino
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European (Finnish)
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European (Non-Finnish)
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allele num: 66738
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African
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Other
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South Asian
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DP
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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FS
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MQRankSum
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InbreedingCoeff
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QD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

European (Finnish)
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Latino
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European (Non-Finnish)
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Other
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African
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South Asian
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QD
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MQ
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ClippingRankSum
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InbreedingCoeff
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FS
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DP
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ReadPosRankSum
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VQSLOD
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MQRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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European (Non-Finnish)
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East Asian
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European (Finnish)
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Other
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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

ClippingRankSum
type: SiteQuality
SIO_000300: 8.080000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.48e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.359e0

DP
type: SiteQuality
SIO_000300: 3.6804e6

MQRankSum
type: SiteQuality
SIO_000300: 1.57e0

FS
type: SiteQuality
SIO_000300: 5.41e-1

QD
type: SiteQuality
SIO_000300: 1.197e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.06e-1

MQ
type: SiteQuality
SIO_000300: 5.829e1

GenotypeDepth
all individuals: 2907
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4700
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5599
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2996
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4023
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40753
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 2801
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2790
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2168
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2130
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3021
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 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

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: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
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: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.79e-1

MQ
type: SiteQuality
SIO_000300: 5.905e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.068e0

VQSLOD
type: SiteQuality
SIO_000300: -1.751e-1

FS
type: SiteQuality
SIO_000300: 7.007e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.286e1

MQRankSum
type: SiteQuality
SIO_000300: 1.88e-1

DP
type: SiteQuality
SIO_000300: 3.680322e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e-1